UNITED STATES
                       SECURITIES AND EXCHANGE COMMISSION
                             Washington, D.C. 20549

                                    FORM 10-K
                Annual Report Pursuant to Section 13 or 15(d) of
                       the Securities Exchange Act of 1934

For the fiscal year ended December 31, 2003.2004.         Commission File No. 0-11178
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                           UTAH MEDICAL PRODUCTS, INC.
                           ---------------------------
             (Exact name of registrant as specified in its charter)

                     Utah                                87-0342734
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          (State or other jurisdiction of            (I.R.S. Employer
           incorporation or organization)            Identification No.)

                               7043 South 300 West
                                Midvale, UT 84047
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                    (Address of principal executive offices)

Registrant's telephone number, including area code:   (801) 566-1200
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Securities registered pursuant to Section 12(b) of the Act:
                                                             None
                                                            ----------

Securities registered pursuant to Section 12(g) of the Act:

                               Title of each Class
                               -------------------
                          Common Stock, $.01 par value
                         Preferred Stock Purchase Rights

  Indicate by check mark whether the registrant (1) has filed all reports
required to be filed by Section 13 or 15(d) of the Securities Exchange Act of
1934 during the preceding 12 months (or for such shorter period that the
registrant was required to file such reports) and; (2) has been subject to such
filing requirements for the past 90 days.  Yes  [X]X    No
                                               [ ]---

  Indicate by check mark if disclosure of delinquent filers pursuant to Item 405
of Regulation S-K (229.405 of this chapter) is not contained herein, and will
not be contained, to the best of registrant's knowledge, in definitive proxy or
information statements incorporated by reference in Part III of this Form 10-K
or any amendment to this Form 10-K. [X]X
                                   ---

  Indicate by check mark whether the registrant is an accelerated filer (as
defined in Rule 12b-2 of the Act). Yes  X  No
                                       ---

  State the aggregate market value of the voting and non-voting common equity
held by non-affiliates computed by reference to the price at which the common
equity was last sold, or the average bid and asked price of such common equity,
as of the last business day of the registrant's most recently completed second
fiscal quarter. As of June 30, 2003,2004, the aggregate market value of the voting
and nonvoting common equity held by nonaffiliates of the registrant was
$86,897,000.

  The aggregate market value of the voting stock held by non-affiliates of the
registrant as of March 5, 2004,4, 2005, based on NASDAQ/NMS closing price: $106,259,000.$83,079,000.

  The number of shares outstanding of the registrant's common stock as of
March 5, 2004: 4,482,6284, 2005: 4,090,061

                       DOCUMENTS INCORPORATED BY REFERENCE

  List herein the documents incorporated by reference: The Company's definitive
proxy statement for the Annual Meeting of Shareholders is incorporated by
reference into Part III, Items 10, 11, 12, and 13 of this Form 10-K.





                               
INDEX TO FORM 10-K PAGE PART I Item 1. Business ......................................................................... 1 Item 2. Properties ...................................................................... 12 Item 3. Legal Proceedings ............................................................... 12 Item 4. Submission of Matters to a Vote of Security Holders ............................. 12 PART II Item 5. Market for the Registrant's Common Equity and Related Stockholder Matters ....... 13 Item 6. Selected Financial Data ......................................................... 14 Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations .................................................................... 16 Item 7A. Quantitative and Qualitative Disclosures about Market Risk ...................... 25 Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure .......................................................... 26 Item 9A. Controls and Procedures ......................................................... 27 PART III Item 10. Directors and Executive Officers of the Registrant .............................. 28 Item 13. Certain Relationships and Related Transactions .................................. 28 PART IV Item 14. Exhibits, Financial Statements Schedules, and Reports on Form 8-K ............... 29 Index to Consolidated Financial Statements ....................................................INDEX TO FORM 10-K ------------------ PAGE ---- PART I Item 1 Business ........................................................ 1 Item 2 Properties ...................................................... 11 Item 3 Legal Proceedings ............................................... 12 Item 4 Submission of Matters to a Vote of Security Holders ............. 12 PART II Item 5 Market for the Registrant's Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities ................................. 13 Item 6 Selected Financial Data ......................................... 15 Item 7 Management's Discussion and Analysis of Financial Condition and Results of Operations ............................ 17 Item 7A Quantitative and Qualitative Disclosures about Market Risk ...... 25 Item 8 Financial Statements and Supplementary Data ..................... 25 Item 9 Changes in and Disagreements with Accountants on Accounting and Financial Disclosure ............................ 25 Item 9A Disclosure Controls and Procedures .............................. 25 Item 9B Other Information ............................................... 25 PART III Item 10 Directors and Executive Officers of the Registrant .............. 26 Item 11 Executive Compensation .......................................... 26 Item 12 Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters ..................... 26 Item 13 Certain Relationships and Related Transactions .................. 26 Item 14 Principal Accountant Fees and Services .......................... 26 PART IV Item 15 Exhibits and Financial Statements Schedules ..................... 27 Signatures ...................................................... 29 Index to Consolidated Financial Statements ................................ F-1
Management's Report on Internal Control Over Financial Reporting .......... F-2 Report of Independent Registered Public Accounting Firm on Management's Assessment on Internal Control Over Financial Reporting ................. F-3 Report of Independent Registered Public Accounting Firm on Financial Statements .................................................... F-5 PART I ------ ITEM I - BUSINESS.BUSINESS Utah Medical Products, Inc. ("UTMD" or "the Company") is in the business of producing high quality cost-effective healthcare industry devices that are predominantly proprietary, disposable and for hospital use. Success depends on 1) recognizing needs of clinicians and patients, 2) rapidly designing or acquiring economical solutions that gain regulatory approval, 3) reliably producing products that meet those clinical needs, and then 4) selling through a) UTMD's own direct channels into markets where the Company enjoys an established reputation and has a critical mass of sales and support resources, or b) establishing relationships with other medical companies that have the proper resources to effectively introduce and support the Company's products. UTMD's success in providing reliable solutions comes from its proven ability to integrate a number of engineering and technical disciplines in electronics, software, mechanical packaging, instrumentation, plastics processing and materials. The resulting proprietary products represent significant incremental improvements over preexisting clinical tools. UTMD's experience is that, in the case of labor-saving devices, the improvement in cost-effectiveness of clinical procedures also leads to an improvement in overall healthcare including lower risk of complications. UTMD markets a broad range of medical devices used in critical care areas, especially the neonatal intensive care unit (NICU) and the labor and delivery (L&D) department in hospitals, as well as products sold to outpatient clinics and physician's offices. The opportunity to apply solutions to recognized needs results from an excellent core of practicing clinicians who introduce ideas to the Company, and key employees who are both clinical applications savvy and development engineering adept. UTMD's products are sold directly to end users in the U.S. domestic market by the Company's own direct sales representatives and independent manufacturers' representatives. In addition, some of UTMD's products are sold through specialty distributors, national hospital distribution companies and other medical device manufacturers. Internationally, products are sold through other medical device companies and through independent medical products distributors. UTMD has representation in all major developed countries with approximately 100 international distributors. Negative factors that may adversely impact future performance include managed care reforms or hospital group buying agreements that may limit physicians' ability to choose certain products or procedures, new products introduced by other companies that displace UTMD's products, new product regulatory approval delays, changes in the Company's relationships with distribution partners, and loss of key personnel. UTMD was formed as a Utah corporation in 1978. UTMD publicly raised equity capital one time in 1982. In 1995, Utah Medical Products Ltd., a wholly-owned subsidiary located in Ireland, was formed to establish an international manufacturing capability. In 1997, UTMD purchased Columbia Medical, Inc. (CMI), a Redmond, Oregon company specializing in silicone injection molding, assembly and marketing vacuum-assisted obstetrical delivery systems. In July, 1998 UTMD acquired the neonatal product line of Gesco International, a subsidiary of Bard Access Systems and C.R. Bard, Inc. On March 8, 2000, UTMD returned to the Nasdaq Stock Market after trading on the New York Stock Exchange for about 3 years. The Company was previously listed on Nasdaq for 14 years. The Company's corporate offices are located at 7043 South 300 West, Midvale, Utah 84047 USA. The corporate telephone number is (801) 566-1200. European operations are located at Garrycastle Industrial Estate,Athlone Business and Technology Park, Athlone, County Westmeath, Ireland. The telephone number in Ireland is (90) 647-3932. CMI's mailing address is 1830 S.E. 1st, Redmond, Oregon 97756. The phone number in Oregon is (541) 548-7738. 1-1- PRODUCTS - -------- Labor and Delivery/ Obstetrics: - ------------------------------ Fetal Monitoring Accessories. About 60% of births are considered "higher risk" due to lack of prenatal care, among other factors. In many of these births, labor may become complicated and does not progress normally. The obstetrician must assess progression of labor to be able to intervene with drug therapy, infuse a solution to augment amniotic fluid, or ultimately if necessary, perform a Cesarean Section procedure, and be prepared for complications following childbirth. To assist the physician in assessing fetal well-being, changes in fetal heart rate (FHR) in conjunction with trends in intrauterine pressure are often electronically monitored. UTMD's intrauterine pressure (IUP) catheter product line provides for clinician choices from a traditional fluid-filled system to INTRAN(R) PLUS, the most widely accepted transducer-tipped system. In addition, adjunct FHR electrodes, leg plates, belly bands and chart paper are offered by UTMD to complete a package of fetal monitoring supplies. UTMD's IUP catheters include: - IUP-075 and UTMD's other custom fluid-filled catheter kits utilize a saline-filled catheter that is placed within the uterine cavity, connected to a separate external reusable or disposable transducer. This product package, utilizing double lumen catheters, was the traditional mode of intrauterine monitoring prior to the introduction of INTRAN. An intrauterine pressure change is transmitted through the fluid column to the external pressure transducer. - Introduced in 1987, INTRAN was the first disposable intrauterine pressure catheter that placed the pressure transducer at the pressure source within the uterine cavity. This design eliminated the complicated setup of fluid-filled systems and provided more accurate pressure waveforms. INTRAN I was discontinued in 1995 in favor of the more widely preferred INTRAN PLUS, also covered by UTMD's original INTRAN patent. - INTRAN PLUS was introduced in 1991. The INTRAN PLUS catheter combines the transducer tip concept of INTRAN I with a refined tip design, a zero switch that allows the clinician to verify the reference of the monitor, and a dedicated amnio lumen which provides immediate access to the amniotic fluid environment which may be essentialhelpful in the diagnosis and intervention of certain fetal conditions. In 1996, a viewport enhancement which allows physicians to observe amniotic fluid in a closed system was added to INTRAN PLUS. In 1997, UTMD introduced several variations to address user preferences in tip size and zero switch location. UTMD markets disposable electrodes, catheters and accessories as outlined above, but does not currently market monitors, the electronic capital equipment that process the electrical signals. In addition to products currently offered, UTMD intends to continue to investigate and introduce tools that enhance fetal monitoring techniques, a core area of product development focus. Vacuum-Assisted Delivery Systems (VAD). UTMD's VAD Systems include CMI(R) patented soft silicone bell-shaped birthing cups and patented hand-held vacuum pumps which UTMD believes are the safest products available for use in vacuum-assisted operative deliveries. UTMD's patented soft silicone cup is unique in the industry. A softa bell-shaped cup design should be preferred for fetal well-being in low or outlet fetal stations with occiput anterior presentations, which should represent more than 90% of the cases where VAD is indicated. Operative vaginal deliveries using forceps or vacuum-assisted delivery systems provide knowledgeable physicians with an alternative to C-section intervention. Although there are risks associated with operative vaginal deliveries which represent about 15% of all U.S. hospital births, the procedures are generally regarded as safer for the mother, and at least as safe for the fetus, as abdominal (Cesarean) delivery in comparable clinical situations. UTMD estimates that the VAD operative approach is used for 2 about 8-10% of all U.S. births, with forceps continuing to lose ground as the alternative. UTMD's patented bell-shaped soft silicone TENDER TOUCH(R) cups enjoy a low reported complication rate compared to other vacuum cup designs, as evidenced by the FDA Medical Device Reporting System which reports specific names of products used in hospitals. -2- Other Obstetrical Tools. AROM-COT(TM) is a finger cover with a patented prong design to rupture maternal membranes with less patient pain and anxiety. MUC-X is an aspiration device used immediately after birth to clear neonatal respiratory passages and reduce exposure to potential infections. CORDGUARD(R) is a patented product which unifies the multiple steps of clamping the neonate's cord close to the umbilicus, severing the cord without splattering blood, drawing a clean cord blood sample, and assisting in the removal of the placenta. CORDGUARD's sharpless, closed system reduces the risk of exposure to potentially infected blood, and consequently reduces the high cost of exposure treatment under OSHA and CDC guidelines. In addition, CORDGUARD facilitates obtaining neonatal blood that is otherwise hard to obtain safely and cleanly. Abcorp belts and straps for fetal monitoring by an external tocodynamometer are provided in latex free form in several configurations. Neonatal Intensive Care: - ----------------------- DISPOSA-HOOD(TM) The DISPOSA-HOOD is an infant respiratory hood that is used in the NICU to administer oxygen to neonates and flush CO2 (carbon dioxide) while maintaining a neutral thermal environment critical to proper physiologic responses. The DISPOSA-HOOD, placed over the infant's head, incorporates a round diffusor connection specifically designed to disperse the incoming gases along the inner surfaces of the hood, rather than allowing them to blow directly on the infant's head. The design allows more precise FIO2 (fractional inspired oxygen) control, minimizes convective heat loss from the head and provides optimum flows for elimination of CO2 (carbon dioxide) by ventilation. Because it is a disposable product, it allows for excellent visualization of the underdeveloped infant and prevents cross-contamination. DELTRAN(R) PLUS UTMD's DELTRAN blood pressure monitoring system has been adapted specifically for use in the NICU. The new streamlined version eliminates needles used for blood sampling, avoids the loss of scarce neonatal blood volume and provides a closed system that reduces the risk of infection. The system features excellent visualization of clearing volume and one-handed use. GESCO(R) In the third quarter of 1998, UTMD acquired the neonatal product line of Gesco International, a subsidiary of Bard Access Systems and C.R. Bard, Inc. GESCO, best known for innovative silicone catheters, gained an early distinctive reputation for its focus on the special developmental needs of tiny critically-ill babies. A class of catheters called umbilical vessel catheters (UVC's) are specially designed for administering vital medications and fluids immediately following birth through the infant's umbilical vessel into the inferior vena cava. Because of the neonate's small size and lack of vascular development, there is no better access to vital organs. The catheters are also called umbilical artery catheters (UAC's) when placed in one of the umbilical arteries to measure blood pressure or monitor metabolic processes through blood analysis. In developing its UMBILI-CATH(TM) product line, Gesco pioneered the use of soft, biocompatible silicone catheters, helping to reduce the number of insertions required as well as other complications associated with invasive applications. UTMD has expanded the UVC product line to include catheters made from a patented thermosensitive polyurethane (Tecoflex(R)) that offers many of the flexibility and biocompatibility advantages of silicone after insertion, with the greater rigidity of polyurethane preferred by many clinicians for insertion. In addition, GESCO provides a convenient catheterization procedure tray of implements and supplies necessary to place UVC catheters, as well as perform other similar procedures. 3 The primary distinction of GESCO products is that they arewere developed with the special needs of the neonate in mind, not just cut-down or smaller versions of adult devices. For example, in the case of invasive catheters, the introducer, the soft rounded distal tip, mode of securing to the patient after insertion to avoid migration, luer locking hub with minimal dead space, number of lumens, catheter radiopaque striping for visualization, variations in catheter lengths and diameters and special packaging are all features specially designed for neonates. UTMD continues to modify product features to incorporate current neonatal nurse practitioner preferences. -3- The soft, biocompatible silicone catheter concept had important advantages in other applications including peripherally inserted central venous catheters (PICC lines), enteral feeding tubes, urinary drainage catheters, and chest drainage tubes. GESCO developed and marketed initial versions of all of these neonatal products. In order to keep pace with the trend of caring for smaller babies, UTMD has added smaller diameter versions of its URI-CATH(R) and NUTRI-CATH(R) products. In 2000, UTMD gained FDA premarketing clearance of a new PICC family of products specifically designed to minimize trauma to the critically ill neonate, named PICC-NATE(R). The PICC-NATE product line was designed with the input of experienced neonatal nurse practitioners for use as a long-term indwelling catheter system for single-use, therapeutic central venous infusion of drug solutions, blood products or other fluids and for blood sampling. The soft, strong silicone PICC-Nate comes in two diameter sizes, two types of venipuncture introducers, and two hub configurations and the option of an integral stylet that aides insertion.configurations. In early 2003, UTMD added a Tecoflex polyurethane version that offers many of the flexibility and biocompatibility advantages of silicone after insertion, with the greater rigidity of polyurethane preferred by many clinicians for insertion. Other GESCO specialty products include a disposable peritoneal dialysis set that is a pre-assembled, sterile, closed system, called DIALY-NATE(R); a patented silicone oral protection device used to prevent palatal soft tissue injury by orotracheal tubes, called PALA-NATE(R); and a lumbar sampling kit with a tiny, specially-beveled needle for obtaining cerebral spinal fluid samples, called MYELO-NATE(R). GESCO's first patented product, HEMO-NATE(R), is a disposable filter designed to remove microaggregates from stored blood prior to transfusion into a neonate where any deficiency can have an overwhelmingly negative impact on a neonate's chances for survival, given an under-developed vasculature and small total blood volume. In 2001, UTMD introduced a new filter and an improved blood bag spike for Hemo-Nate, and a needleless version. In 2004,2005, UTMD will continue to improve and expand its neonatal product line, seeking to reinforce a reputation as having the most developmentally-friendly NICU specialty products in the medical device industry. In addition to products already offered and being developed internally, UTMD will look to expand sales through distribution arrangements with other manufacturers, or through selective acquisitions. Gynecology /Urology /Electrosurgery: - ----------------------------------- LETZ(R) System The LETZ System is used to excise cervical intraepithelial neoplasia (CIN) and other lower genital tract lesions related to human papilloma virus (HPV) infections. The electrosurgery procedure with hemostasis has become the standard of care for HPV cervical infection treatment, replacing cold knife scalpel, laser and cryotherapy procedural approaches because it is economical, safe, effective, quick and easy to perform, has fewer potential side effects, and requires little physician training. Most importantly, in contrast to laser (tissue ablation) and cryotherapy (freezing of tissue), LETZ provides a fine tissue specimen for pathological assessment. Therefore, LETZ is effective both as a diagnostic and therapeutic procedure. The LETZ procedure may be performed using local anesthetic in a physician's office, eliminating the time and expense of hospital or surgical center admittance. UTMD's LETZ System includes patented disposable electrodes, the patented FINESSE(R) electrosurgical generator, and other miscellaneous components. A disposable loop electrode used to excise the tissue specimen is a pencil-like tube with a thin tungsten wire loop attached. The loop is available in varying 4 sizes and includes a Safe-T-Gauge(R) that can be positioned so the physician can accurately colposcopically monitor the amount of tissue being excised. UTMD continues to augment its specialty electrodes. For example, the Company introduced a patented conization electrode for deep endocervical disease called C-LETZ(R), designed to limit the removal of healthy tissue margins that might compromise adequate cervical function. UTMD also will continue to provide adapters and other components which allow its market-leading specialty electrodes to be used with other manufacturers' electrosurgical generators. The FINESSE electrosurgical generator is the only generator on the market that contains an integral smoke evacuator, required to filter smoke and vapors that contain potentially hazardous particulate material produced during electrosurgery. FINESSE(R) Generator; Specialty Loop, Ball, and Needle Electrodes; FILTRESSE(R) Evacuator; Other Specialty Electrodes; Other Supplies and Gynecologic Tools. -4- UTMD has FDA clearance to market its electrosurgical system and tools for use in general surgery applications, including dermatology, plastic surgery and otolaryngology. In 2002, UTMD recently introduced a new product line of ultra-fine tipped microdissection needles, called OptiMicro(TM) Needles. The newThese electrosurgical needles are particularly useful in plastic and reconstructive surgery applications. FILTRESSE is a stand-alone surgical smoke filtration system that combines high filtration efficiency, low cost and convenient use in a surgical office setting. Other electrosurgery tools and accessories include disposable electrosurgical pens, dispersive pads, footswitches, filter packs, speculums, retractors, forceps, tenacula and hooks. UTMD acquired the distribution rights to a unique reusable four-way expander system which facilitates access to, and visualization of, the cervix, eliminating the need for less effective specula and lateral retractors. EPITOME(R) EPITOME is a patented electrosurgical scalpel which delivers precise performance in incision and excision with hemostasis while minimizing thermal side effects. Where rapid yet precise dissection of dense tissue is necessary, such as in mammaplasty or abdominoplasty, EPITOME has no peer. An independent study concludes that the EPITOME scalpel provides a significant improvement over older devices in wound healing and patient comfort. EPITOME allows a rapid incision without countertraction, yielding limited morbidity, less post-surgical pain and cosmetically superior results. EPITOME is useful where minimization of thermal tissue injury is important but control of bleeding needed. A patented bendable version of EPITOME with a smaller active electrode was introduced in 1998. Designed to significantly reduce the chance of tissue burns due to inadvertent electrode contact and where a smaller, bent scalpel tip is needed, the bendable EPITOME is of particular value, e.g., to thoracic surgeons in harvesting the internal mammary artery during coronary artery bypass surgery, as well as to otolaryngologists for tonsillectomies. LIBERTY(R) System LIBERTY is a device for the conservative treatment and effective control of urinary incontinence in women. UTMD believes that LIBERTY is the easiest-to-use, most cost effective incontinence treatment available that yields a therapeutic effect, not just a cover-up. LIBERTY consists of a battery operated electrical stimulation unit and an intravaginal electrode probe. This physiotherapy technique, which can be done in the privacy of the home, involves passive strengthening of the periurethral muscles. Pulsed, low voltage, high frequency current is applied primarily to the pudendal neuromuscular tissue causing the pelvic area muscles to contract, leading to better muscle tone. Because electrical stimulation has no known adverse side effects, LIBERTY provides women suffering from mild to moderate incontinence an effective, lower cost and lower risk alternative to more traumatic treatments such as surgery and drug therapy. Since HCFA (Health Care Financing Administration) now called CMS (Center for Medicaid/ Medicare Services) decided in late 2000 to allow reimbursement for electrical stimulation devices, adoption of Liberty has substantially increased. 5 PATHFINDER PLUS(TM) PATHFINDER PLUS is a proprietary endoscopic irrigation device that allows a uro/gyn surgeon to precisely irrigate with the same hand that controls the endoscope, eliminating the need for a separate assistant to irrigate without visualization. ENDOCURETTE(TM) In cooperation with Mayo Clinic, UTMD developed an advanced curette for uterine endometrial tissue sampling in the doctor's office. The sampling procedure is intended primarily to rule out precancer or cancerous change of the uterus in premenopausal women with abnormal uterine bleeding, or women with postmenopausal bleeding. The device is part of a class of catheters designed to be used without dilitation of the cervix and without general anesthetic. The inherent weakness of this type of device, which is related to its small size, is that it may not remove enough tissue of the endometrium for an accurate histologic assessment. The patented tip of the ENDOCURETTE was designed to obtain a more thorough tissue specimen without the need for dilitation, and without an increase in patient discomfort. LUMIN(R) LUMIN(R) is a patented tool developed by UTMD for reliably and safely manipulating the uterus in gynecological laparoscopic procedures. LUMIN combines the strength, range of motion and versatility of the higher end reusable instruments with the lower cost and cleanliness of the inexpensive less functional disposable instruments presently on the market, while at the same time reducing the number of tools needed to move and secure the uterus. -5- Blood Pressure Monitoring: DELTRAN(R) Disposable Pressure Transducer (DPT) In pressure monitoring, a transducer is used to convert physiological (mechanical) pressure into an electrical signal that is displayed on electronic monitoring equipment. UTMD developed, patented and is now distributing its disposable transducer as a stand-alone product, and as a component in sterile blood pressure monitoring kits through direct representatives and other medical companies in the U.S., as well as independent distributors and other medical device companies internationally. Although other large medical companies manufacture and market disposable pressure transducers ("DPTs") under rights to UTMD's technology, theThe Company believes that the DELTRAN DPT which it designed nearly twenty years ago, and currently manufactures, remains the standard in terms of accuracy, reliability and ease of use. UTMD has an automated assembly line which allows the Company to effectively compete with the largestlarger suppliers on the basis of consistent quality and low manufacturing costs. Introduced in 1998, the DELTRAN PLUS provides a closed system for blood sampling, without the use of needles, reducing the risk of an unwanted infection for both the patient and the practitioner. Pressure Monitoring Accessories, Components and Other Molded Parts. Components included in blood pressure monitoring kit configurations include flush devices, stopcocks, fluid administration sets, caps, pressure tubing, interface cables and organizers. The Company sells similar components designed for other medical companiesdevice company applications which incorporate UTMD's technologies and designs. DELTA-CAL(TM) is a calibration device used to check proper functioning of an arterial pressure system. In addition, UTMD sells plastic molded parts on a subcontract basis to a number of medical and non-medical device companies. UTMD believes that this practice helps better utilize its investment in fixed plant and equipment. MARKETING - --------- UTMD competes on the basis of its value-added technologies and cost effective clinical solutions. UTMD believes that a number of its products are strong brands because they are recognized as clinically different. The Company's primary marketing challenge is to keep its customers focused on those differences and their important clinical benefits. Access to the clinical decision-makers, together with the active involvement of clinicians in medical device purchasing decisions, is critical to the Company's success. 6 UTMD's specialty focus, innovation and extensive experience in its specialtyspecialties are important marketing attributes which help assure its ability to successfully compete and survive in a consolidating marketplace where many suppliers are trying to degrade product differences. For U.S. hospitals, which represent about 60% of UTMD's productdevice sales, marketing efforts are complicated and fragmented. Although UTMD's focus is with clinicians who take responsibility for obtaining optimal patient care outcomes, other people are generally administratively responsible for hospital purchasing decisions. DISTRIBUTION - ------------ UTMD believes anotherAn important success factor in the current healthcare industry is access to customers. Although the U.S. hospital supplier environment has been consolidating as a result of group purchasing organizations (GPOs), or their equivalent, establishing long term contracts with large medical device suppliers with diverse product lines in recent years, theirthe financial relationships and true benefits for hospitals has come under increased scrutiny, both by hospitals' managements themselves and by the government. As a potential positive factor to UTMD's future performance, the increased scrutiny may lead to an understanding consistent with UTMD's belief that hospitals mayare not be currently saving money under many of the GPO contracts, andcontracts. In addition, the longer term overall cost of care will be substantially higher, with quality of care lower, as innovative suppliers are excluded from participating in the marketplace. The length of time and number of administrative steps required in evaluating new products for use in hospitals has grown substantially in recent years. As a potential negative factor to future performance, as UTMD introduces new products -6- it believes are safer and more effective, it may find itself excluded from certain customers because of the existence of long term supply agreements for existing products. UTMD may also be unable to establish viable relationships with other medical device companies that do have access to users but lack an interest in the Company's approach. In the United States, UTMD sells its products primarily through its own directly employed sales force.force and through selective independent manufacturer representatives. The current network of direct representatives is employed to concentrate on select market applications for UTMD products and to provide properwhere customer training and support.support are important. As of March 2004,2005, the U.S. direct sales force is comprised of both outside territory representatives operating remotely geographically, as well asand inside representatives who operate by telephone.telephone from corporate offices. Direct representatives are trained to understand the medical procedures being performed within UTMD's clinical focus. Through the use of its one-on-one contacts with physicians and other clinicians directly involved in patient care, the direct sales force positions UTMD to gain market leadership with solutions to clinical problems. In addition to its direct representatives, UTMD utilizes third party consulting clinical specialists to augment its customer training programs. When hospital customers request it, UTMD provides its products through national distribution companies, also known as Med/Surg distributors. Sales to Med/Surg distributors currently comprise aboutless than 10% of total domestic sales. In contrast, seveneight years ago, national distributors and independent stocking distributors in the U.S. represented more than 65% of UTMD's direct domestic Ob/Gyn business. In addition to the above traditional distribution methods,sales approaches, UTMD encourages customers to take advantage of fast and easy direct online ordering at www.order.utahmed.com. UTMD's website provides all the convenience of e-commerce expected ofdemonstrated on other sites. UTMD's experience to date with third party Internet-based exchanges suggests that they do not warrant a significant investment of UTMD resources until customers show more interest in their use. Additionally, UTMD sells component parts to medical companies for use with their product lines. This OEM distribution channel effort is simply maximizing utilization of manufacturing resources that are otherwise needed for UTMD's 7 primary business, and does not compete with or dilute UTMD's direct distribution and marketing programs. Internationally, the Company sells its products through about 80 regional distributors and through about 20 OEMs (other medical device manufacturers). The international business is driven by the initiative and resourcefulness of these distributors. UTMD's Internet website www.utahmed.com is a frequent conduit for international customer inquiries. NEW PRODUCT DEVELOPMENT - ----------------------- New product development is a key to UTMD's market identity as an innovator. Product development takes three interrelated forms: 1) improvements, enhancements and extensions of current product lines in response to clinical needs or clinician requests, 2) invention of devices that allow significantly different methods of performing medical procedures, representing a quantum improvement in safety, efficacy and/or cost of care, and 3) acquisitions of products or technology from others. Because of UTMD's reputation as a successful innovator, its financial strength and its established clinician user base, it enjoys a substantial flowinflow of new product ideas. Internal development, joint development, product acquisitions and licensing arrangements are all included as viable options in the investigation of opportunities. Only a small percentage of ideas survive feasibility screening. For internal development purposes, projects are assigned to a project manager who assembles an interdisciplinary, cross-functional development team. The team's objective is to have a clinically proven, manufacturable and FDA released product ready for marketing by a specific date. Approximately ten projects on the average, depending on the level of resources required, are underway at UTMD at any given time. More than 50% of assigned projects do not succeed in attaining a product that meets all of the Company's criteria. In particular, this includes a product that is highly reliable, easy to use, cost-effective, safe, useful and differentiated from the competition. Once a product is developed, tooled, fully tested and cleared for marketing by the FDA, there remains a reasonable probability it cannot be successfully marketed for -7- any number of reasons, not the least of which is being beaten to the market by a competitor with a better solution, or not having access to users because of limitations in marketing and distribution resources or exclusionary contracts of GPOs. UTMD's current product development projects are in three areas of focus: 1) obstetrics/ fetal monitoring, 2) neonatal intensive care, and 3) specialized procedures for the assessment and treatment of cervical/uterine disease. UTMD has had 7 patents issued in the last five years. Internal product development expenses are expected to be in the range of 1-2% of sales in 2004.2005. In 2003,2004, UTMD spent $288$292 (in thousands) on internal product development activities, or 1.1% of sales. In addition, the Company invested $120$10 in new technology rights which have not resulted in a marketable product yet. In 20022003 and 2001,2002, internal new product development expenses were $285 (1.0%$288 (1.1% of sales) and $364 (1.3%$285 (1.0% of sales), respectively. EMPLOYEES - --------- At December 31, 2003,2004, the Company had 211206 employees. The average tenure of all of UTMD's employees is aboutover eight years. The Company's continued success will depend to a large extent upon its ability to retain skilled employees. No assurances can be given that the Company will be able to retain or attract such employees in the future, although management is committed to providing an attractive environment in which creative and high achieving people wish to work. To the best of the Company's knowledge, none of the Company's officers or directors is bound by restrictive covenants from prior employers that limit their ability to contribute to UTMD's programs. All professional employees sign a code of conduct and a confidentiality and non-compete agreement, as a condition of employment, and as consideration for receipt of stock option awards and participation in the management bonus program. All employees participate in 8 performance-based bonus programs. None of the Company's employees is represented by labor unions or other collective bargaining groups. PATENTS AND TECHNOLOGY LICENSES - ------------------------------- The Company owns or exclusively licenses thirty-one unexpired patents, and is the licensee of certain other technology. There can be no assurance, however, that patents will be issued with respect to any pending applications, that marketable products will result from the patents or that issued patents can be successfully defended in a patent infringement situation. The ability of the Company to achieve critical mass in the marketplace depends in large part on the protection afforded by its patents. In cases where competitors introduce products that may infringe on UTMD's technology, the Company has an obligation to its shareholders to defend its intangible property to the extent that it can afford to do so. In January 2002, a jury in the U.S. Federal District Court for the District of Utah rendered a verdict in favor of UTMD that the Tyco/KendalloLTP Softrans 4000 Intrauterine Pressure Catheter literally infringes UTMD's Patent No. 4,785,822 for inventions relating to a "Disposable Intracompartmental Pressure Transducer." UTMD markets the Intran(R) Plus which practices this patent. The patent infringement lawsuit had been filed in early 1997. In September 2002, the US Federal District Court issued a formal judgment awarding UTMD approximately $23 million in damages and accrued interest. Additional damages for infringing product sold by Tyco after the January verdict were to be determined by the Court at a later date. In addition, the Court issued a permanent injunction against Tyco prohibiting the manufacturing, marketing, selling and/or otherwise distributing of the 4000 Softrans IUPC for the duration of UTMD's patent. Tyco/Kendall filed an appeal to the decision. In December 2003, the United States Court of Appeals for the Federal Circuit upheld in entirety the District Court's judgment. In January 2004, UTMD received $31 million from Tyco/Kendall, including post judgment augmented damages and interest. One other patent infringement lawsuit where UTMD is plaintiff is currently pending. As a matter of policy, UTMD has acquired and will continue to acquire the use of technology from third parties that can be synergistically combined with UTMD proprietary product ideas. During 2003,2004, ongoing royalties included in cost of goods sold were $3 (in thousands). Other royalties have been previously paid as -8- a lump sum, or are incorporated into the cost of supplied components which practice certain patents of third parties. Also as a matter of policy, UTMD licenses its proprietary technology to others in circumstances where licensing does not directly compete with UTMD's own marketing initiatives. During 2003,2004, the Company received $450 in royalty income, compared to $450the same as in 20022003 and $452 in 2001.2002. Non-operating income remains a significant portion of UTMD's earnings. UTMD's future financial performance also depends on the marketing ability of other companies that license UTMD's technology. GOVERNMENT REGULATION - --------------------- UTMD's products are subject to regulation by the U.S. Food & Drug Administration ("FDA"), as well as other regulatory bodies globally. The FDA has authority to regulate the marketing, manufacturing, labeling, packaging and distribution of medical productsdevices in the U.S. In addition, requirements exist under other federal laws and under state, local and foreign statutes that may apply to the manufacturing and marketing of the Company's products. All manufacturers of medical devices must register with the FDA and list all medical devices produced by them. The listing must be updated annually. In addition, prior to commercial distribution of some devices for human use, a manufacturer must file a notice with the FDA, setting forth certain information regarding the safety and effectiveness of the device that is acceptable in content to the FDA. 9 Devices which are classified in Class I are subject only to the general controls concerning adulteration, misbranding, good manufacturing practices, record keeping and reporting requirements. Devices classified in Class II must, in addition, comply with special controls or performance standards promulgated by the FDA. The Company believes all of its present products are Class I or Class II productsdevices and that the Company is in full compliance with all applicable material performance standards as well as FDA cGMP (current good manufacturing practice) quality standards, record keeping and reporting (QSR).reporting. In 2003 the FDA began withholding export certificates from UTMD, which action was part of an unresolved disagreement regarding the issuance of a QSR Warning Letter by FDA to UTMD in September 2001. Export certificates are non-bindingnonbinding letters assuring other countries that a company is in compliance with FDA regulations. The export certificates have now been withheld for many months while UTMD distributes its products in the U.S. without any FDA interference.restriction, or any FDA claim that UTMD's products are unsafe or ineffective. The Company strongly believes that there is no reasonable basis for this decision,denial. On August 10, 2004, the FDA issued a press release announcing it would seek an injunction against UTMD until it had corrected alleged "deviations" from the Quality System Regulation, 21 CFR Part 820 (QSR). UTMD responded with several press releases shortly following the FDA's announcement, and has filed two lawsuitswith periodic public updates since then. The FDA press release and filing of the action in the U.S. FederalDistrict Court for the District of Utah caused significant disruption to UTMD's business, in part because of inappropriate activities of UTMD competitors incorrectly telling customers that the Company has been, or was about to be, shut down. As a matter of fact, through the date of this report: 1) UTMD continues to manufacture and distribute all of its products worldwide without any regulatory restriction, 2) there has been no mandated recall or any other regulatory enforcement action that restricts customers from using UTMD's products, 3) There has not been, and is not now, any allegation by the FDA that UTMD's products are not safe or effective, 4) there is no FDA claim of defective products or products not conforming to specifications, and 5) the proven extremely low product liability risk using UTMD's products has not changed. On November 16, 2004 UTMD announced that an effort to rectifyFDA enforcement official, officially designated as the situation.knowledgable FDA representative, testified under oath that the FDA is not claiming in the lawsuit that UTMD's devices are either unsafe or ineffective. Discovery in the lawsuit is ongoing at the date of this report, with a pre-trial conference scheduled for June 20, 2005. As part of its expert witness testimony in the lawsuit, the Company has provided independent QSR expert certification that UTMD is in substantial compliance with the QSR. (See Item 3. - Legal Proceedings.) -9- In 1994, UTMD received certification of its quality system under the ISO 9001/EN 46001 standards ("ISO" stands for "International Organization of Standardization") which wasit maintained until December 2003. BecauseIn October 2003, UTMD's Utah facility was initially certified under the more stringent ISO 13485 standard for medical devices, which it currently maintains. UTMD's Ireland facility is certified under the concomitant ISO 13488 standard. The U.S. FDA QSR was developed in harmony with the ISO standards are in perpetual modification,standards. UTMD has remainedremains on a continuous periodic audit schedule by its independent notified body in order to stay abreast ofcurrent with international regulatory standards. In October 2003, UTMD's Utah facilitystandards, and retain its certification. The most recent audit was certified under the more stringent ISO 13485 standard for medical devices. UTMD's Ireland facility is now certified under ISO 13488.conducted in November 2004. UTMD has received formal product certificationcertifications allowing the use of the CE Mark (demonstrates proof of compliance with the European Community's productISO standards) for essentially all of its products. SOURCES AND AVAILABILITY OF RAW MATERIALS - ----------------------------------------- Most of the components which the Company purchases from various vendors are readily available from a number of sources. Alternate sourcing of various components is continually underway. Vendors are qualified by Corporate Quality Assurance. The Company has a vendor quality monitoring program that routinely checks all incoming material for conformance to specifications. EXPORTS - ------- Revenues from customers outside the U.S. in 20032004 were (in thousands) $5,872 (22%$6,029 (23% of total sales), as compared to $5,872 (22% of total sales) in 2003, and $5,735 (21% of total sales) in 2002, and $5,202 (19% of total sales) in 2001.2002. Blood pressure monitoring products represented 67% of international sales in both 2004 and 2003, compared to 70% in 2002 and 67% in 2001.2002. International Ob/Gyn and neonatal product sales were $2,019 in 2004, compared to $1,930 in 2003 compared toand $1,743 in 2002 and $1,718 in 2001.2002. For financial information by geographical area, please see Notes 1,41, 4 and 9 to the Consolidated Financial Statements. UTMD seesregards the international marketplace as one of the important elements of its growth strategy. UTMD is keenly aware that not only are international markets different from the U.S. market, but also that each country has its own set of driving influences that affects the dynamics of the nature of care given and medical devices used. In 1996 UTMD completed construction of a manufacturing facility in Athlone, County Westmeath, Ireland. The facility offers a number of advantages: 1) from a marketing point of view, faster response to European Union customers, including a better understanding of customized needs, less costly distribution and duty-free access to over 350 million patients; 2) from a regulatory point of view, faster new product introductions; and 3) from a manufacturing point of view, reduced dependence on one manufacturing site and increased capacity at existing U.S. facilities. 10 BACKLOG - ------- As a supplier of primarily disposable hospital products, the nature of UTMD's business necessitates being very responsive to customer orders and delivering products quickly. Virtually all direct shipments to end users are accomplished within one week of receipt of customer purchase order. Backlog shippable in less than 60 days was approximately $0.3 million as of both January 1, 20042005 and January 1, 2003.2004. SEASONAL ASPECTS - ---------------- The Company's business is generally not affected by seasonal factors. PRODUCT LIABILITY RISK MANAGEMENT - --------------------------------- The risk of product liability lawsuits is a negative factor in UTMD's business because UTMD's products are frequently used in inherently life threatening situations to help physicians achieve a more positive outcome than what might otherwise be the case. In any lawsuit against a company where an individual plaintiff suffers a permanent physical injury, a possibility of a large award for damages exists whether or not a causal relationship exists. However, no such damages have been awarded against UTMD in its 25 year history. -10- UTMD is self-insured for product liability risk and reserves funds against its current performance on an ongoing basis to provide for its defense should any lawsuits be filed. The best defense the Company has is the consistent conformance of its proven safe and effective products to specifications. In the last tentwelve years, UTMD has been named as a defendant, along with each attending physician and hospital, in four product liability lawsuits. All four were related to operative vaginal deliveries where a VAD product was used. The VADS products did conform to specifications. UTMD was ultimately dismissed as a defendant in the lawsuits, and legal costs were not material to performance. During the same period of time, no other UTMD products were the subject of a product liability lawsuit. There are currently no product liability lawsuits in which UTMD is a defendant. FORWARD LOOKING INFORMATION - --------------------------- This report contains certain forward-looking statements and information relating to the Company that are based on the beliefs of management as well as assumptions made by management based on information currently available. When used in this document, the words "anticipate," "believe," "project," "estimate," "expect," "intend" and similar expressions, as they relate to the Company or its management, are intended to identify forward-looking statements. Such statements reflect the current view of the Company respecting future events and are subject to certain risks, uncertainties and assumptions, including the risks and uncertainties stated throughout the document. Although the Company has attempted to identify important factors that could cause the actual results to differ materially, there may be other factors that cause the forward statement not to come true as anticipated, believed, projected, expected, or intended. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may differ materially from those described herein as anticipated, believed, projected, estimated, expected or intended. General risk factors that may impact the Company's revenues includeinclude: the market acceptance of competitive products,products; administrative practices of group purchasing organizations,organizations; obsolescence caused by new technologies,technologies; the possible introduction by competitors of new products that claim to have many of the advantages of UTMD's products at lower prices,prices; the timing and market acceptance of UTMD's own new product introductions,introductions; UTMD's ability to efficiently and responsively manufacture its products, including the possible effects of lack of performance of suppliers,suppliers; success in gaining access to important global distribution channels,channels; budgetary constraints,constraints; the timing of regulatory approvals for newly introduced products,products; regulatory intervention in current operations, including the current action filed by the Justice Department on behalf of the FDA against UTMD in the U.S. District Court for the District of Utah (see Government Regulation, above); and third party reimbursement of health care costs of customers. 11 Risk factors, in addition to the risks outlined in the previous paragraph and elsewhere in this report that may impact the Company's assets and liabilities, as well as cash flows, includeinclude: risks inherent to companies manufacturing products used in healthcare, including claims resulting from the improper use of devices and other product liability claims,claims; defense of the Company's intellectual property,property; productive use of assets in generating revenues,revenues; management of working capital, including inventory levels required to meet delivery commitments at a minimum costcost; and timely collection of accounts receivable. Additional risk factors that may affect non-operating income includeinclude: the continuing viability of the Company's technology license agreements,agreements; actual cash and investment balances,balances; asset dispositionsdispositions; and acquisition activities that may require external funding. ITEM 2 - PROPERTIES Office and Manufacturing Facilities. The Company's current operations are located in an 100,000 square foot facility in Midvale, Utah, a suburb of Salt Lake City, a 20,000 square foot facility in Redmond, Oregon, and a 77,000 square foot facility in Athlone, County Westmeath, Ireland. UTMD owns its property and facilities in Utah and Ireland, with the exception of a long-term lease on one section of its Midvale parking lot. The Oregon facility is leased. -11- UTMD is a vertically-integrated manufacturing company. Capabilities include silicone and plastics-forming operations including injection molding, insert and over-molding, thermoforming and extrusion; sensor production; manual and automated assembly of mechanical, electrical and electronic components; parts printing; various testing modalities; advanced packaging in clean room conditions; and a machine shop for mold-making and fabrication of assembly tools and fixtures. Capabilities also include an R&D laboratory for both electronic and chemical processes, software development resources, communications and computer systems networked real time internationally, and administrative offices. ITEM 3 - LEGAL PROCEEDINGS The Company may be a party from time to time in routine litigation incidental to its business. Presently, there is no such routine litigation ongoing. On August 9, 2004, the United States of America filed a lawsuit in The outcomesUnited States District Court, Central District of lawsuitsUtah v. UTMD, Kevin L. Cornwell, Chairman & CEO, and Ben D. Shirley, Vice President, Product Development & Quality Assurance. The presiding judge is Judge Bruce R. Jenkins. The government (FDA) is seeking a permanent injunction from alleged deviations of the Quality System Regulation (QSR). The FDA is not seeking a preliminary injunction. The FDA is not claiming that the Company's devices are unsafe or ineffective, or do not meet predetermined specifications. UTMD maintains that it has been and is in substantial compliance with all applicable government regulations. The FDA has the burden to prove its allegations. UTMD was served with the complaint on August 12, 2004. On August 10, the FDA released an announcement on its official website regarding filing the lawsuit which are currently pending arecontained a personal quotation from Acting Commissioner Lester Crawford which UTMD believes confused and upset people who use UTMD's devices, and thereby harmed UTMD's commerce and shareholder value. The FDA makes allegations of violations/ deviations in hundreds of Warning Letters it issues to medical device firms annually. Yet, it is rarely challenged to prove these allegations. There is not projectedand never has been an imminent public health risk relating to haveuse of UTMD's products. The FDA has a materially adverse effectvariety of remedies to address device risks without any resort to the courts. None of those remedies has ever been applied to any UTMD device, because none has been justified. Despite statements in the media otherwise, the FDA Denver District Office shut off dialogue with UTMD after 2001 while it performed inspection after inspection in an attempt to build a case. The case that was finally filed involves alleged QSR violations that the agency has been unable to substantiate, despite an effort coordinated by the CDRH including four comprehensive inspections, some involving "national expert" FDA inspectors. An independent expert, a nearly thirty year FDA compliance veteran and former District Director, retained by UTMD, has alleged misconduct within FDA. On February 1, 2005, the U.S. Court granted UTMD's motion to file a counterclaim for abuse of process. Please review UTMD's SEC 8-K disclosures (a link is available on UTMD's financial condition or results of operations. Please refer to the GOVERNMENT REGULATION section on pages 9-10website at http://utahmed.com/sec.htm) for a more complete description of a legal action UTMD filed beginning in 2003 againstUTMD's position regarding its dispute with the FDA. ITEM 4. - SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS No matter was submitted to a vote of security holders through the solicitation of proxies or otherwise during the fourth quarter of the fiscal year covered by this report. [Remainder of Page Intentionally Left Blank] 12-12- PART II ------- ITEM 5 - MARKET FOR THE REGISTRANT'S COMMON EQUITY, AND RELATED STOCKHOLDER MATTERS.MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES Market Information. UTMD's common stock began trading (again) on the Nasdaq National Market (symbol:UTMD) on March 8, 2000. Betweenin 1983. From December 26, 1996 anduntil March 7, 2000, UTMD traded on the New York Stock Exchange (symbol: UM). Previous to December 26, 1996,Since March 8, 2000, UTMD has again traded on the Nasdaq National Market under the UTMD symbol.Market. The following table sets forth the high and low sales price information as reported by Nasdaq for the periods indicated: 2004 2003 2002-------------------- -------------------- High Low High Low ---- ---- ---- ---------- ------ ------ ------ 1st Quarter $26.45 $23.52 $19.35 $17.41 $16.36 $12.51 2nd Quarter 27.19 23.80 20.87 18.10 16.35 14.90 3rd Quarter 27.00 16.02 24.99 20.05 17.04 13.48 4th Quarter 23.45 17.50 26.30 21.00 20.07 16.55 Stockholders. The approximate number of beneficial stockholders of UTMD's common stock as of March 4, 2005 was 3,100. Dividends. On May 10, 2004, UTMD announced that it would begin paying a quarterly cash dividend. The following sets forth cash dividends declared and paid on UTMD common stock over the past two years: Record Date Payable Date Per Share Amount ----------- ------------ ---------------- June 16, 2004 July 5, 2004 was 3,300. Dividends.$0.15 September 16, 2004 October 5, 2004 0.15 December 16, 2004 January 5, 2005 0.15 ---- 2004 total paid $0.30 2003 total paid None Issuer Purchases of Equity Securities. The Company does not currently intend to pay cash dividends onfollowing table details purchases by UTMD of its own securities during fourth quarter 2004.
Total Number of Maximum Number (or Shares Purchased Approximate Dollar Total Number Average as Part of Publicly Value) of Shares that of Shares Price Paid Announced Plans May be Purchased Under Period Purchased (1) per Share or Programs (1) the Plans or Programs (1) - ------------------- ------------- ---------- ------------------- ------------------------- 10/01/04 - 10/31/04 233,200 $ 17.61 233,200 11/01/04 - 11/30/04 6,000 17.96 6,000 12/01/04 - 12/31/04 15,488 21.92 15,488 - ------------------- ------------- ---------- ------------------- ------------------------- Total 254,688 $ 17.88 254,688
(1) In fourth quarter 2004 UTMD repurchased an aggregate of 254,688 shares of its common stock at an average cost of $17.88 per share pursuant to a continued open market repurchase program initially announced in August 1992. Since 1992 through 2004, the foreseeable future. It isCompany has repurchased 5,979,792 shares at an average cost of $10.70 per share including broker commissions and fees in open market transactions. In addition, the present intentionCompany conducted tender offer transactions in -13- which it purchased an additional 2,775,742 shares at an average cost of $9.76 per share including fees and administrative costs. In total, UTMD has repurchased over 8.7 million of its shares at an average price of $10.40 per share since 1992. To complete the picture relating to current shares outstanding, since 1992 the Company's employees and directors have exercised and purchased 1.4 million option shares at an average price of $6.24 per share. All options were awarded at the market value of the Company to use current cash and investment balances and earnings to finance future growth, for selective infusionsstock on the date of technological, marketing or product manufacturing rights to broaden the Company's product offerings, and for continuedaward. The frequency of UTMD's open market share repurchases whendepends on the availability of sellers and the price of the stock remains undervalued.stock. Since the conclusion of its November 2002 tender offer, the Company has repurchased shares on a total of thirty-nine trading days, about 8% of the total trading days available. The board of directors has not established an expiration date or a maximum dollar or share limit for UTMD's continuing and long term pattern of open market share repurchases. The purpose of UTMD's ongoing share repurchases is to maximize the value of the Company for its continuing shareholders, and maximize its return on shareholder equity by employing excess cash generated by effectively managing its business. UTMD does not intend to repurchase shares that would result in terminating its Nasdaq National Market listing. [Remainder of Page Intentionally Left Blank] 13-14- ITEM 6 - SELECTED FINANCIAL DATA.DATA (in thousands, except per share data) The following selected consolidated financial data of UTMD and its subsidiaries for the five years ended December 31, 2003,2004, are derived from the audited financial statements and notes of UTMD and its subsidiaries, certain of which are included in this report. The selected consolidated financial data should be read in conjunction with UTMD's Consolidated Financial Statements and the Notes included elsewhere in this report.
Year Ended December 31 ---------------------- 2003 2002 2001 2000 1999 ---- ---- ---- ---- ---- Net Sales $27,137 $27,361 $26,954 $27,193 $29,444 Net Income 20,761 7,165 5,934 5,373 5,468 Earnings Per Common Share - (Diluted) 4.25 1.36 1.14 .90 .76 Total Assets 49,694 23,387 23,572 25,423 27,756 Working Capital 21,405 5,437 5,400 5,418 5,877 Long-term Debt 0 4,956 2,501 10,000 5,934 Cash Dividends Per Common Share None None None None None Quarterly Data for 2003 ----------------------- First Quarter Second Quarter Third Quarter Fourth Quarter ------------- -------------- ------------- -------------- Net Sales $6,877 $6,840 $6,761 $6,659 Gross Profit 3,977 4,033 3,979 3,902 Net Income 1,788 1,837 1,861 15,274 Earnings Per Common Share - (Diluted) .37 .38 .38 3.10 Quarterly Data for 2002 ----------------------- First Quarter Second Quarter Third Quarter Fourth Quarter ------------- -------------- ------------- -------------- Net Sales $6,705 $6,800 $7,005 $6,854 Gross Profit 3,816 3,917 4,079 3,951 Net Income 1,712 1,785 1,883 1,785 Earnings Per Common Share (Diluted) .32 .33 .36 .35 14
Year Ended December 31 ---------------------- 2004 2003 2002 2001 2000 ---- ---- ---- ---- ---- Net Sales $26,485 $27,137 $27,361 $26,954 $27,193 Net Income 10,220 20,761 7,165 5,934 5,373 Earnings Per Common Share - (Diluted) 2.19 4.25 1.36 1.14 .90 Total Assets 41,262 49,694 23,387 23,572 25,423 Working Capital 20,194 21,405 5,437 5,400 5,418 Long-term Debt 0 0 4,956 2,501 10,000 Cash Dividends Per Common Share 0.30 None None None None Quarterly Data for 2004 ----------------------- First Second Third Fourth Quarter Quarter Quarter Quarter ------- ------- ------- ------- Net Sales $6,616 $6,827 $6,670 $6,372 Gross Profit 3,850 3,934 3,779 3,503 Net Income 5,175 1,841 1,807 1,397 Earnings Per Common Share - (Diluted) 1.07 .38 .39 .32 Quarterly Data for 2003 ----------------------- First Second Third Fourth Quarter Quarter Quarter Quarter ------- ------- ------- -------- Net Sales $ 6,877 $ 6,840 $ 6,761 $ 6,659 Gross Profit 3,977 4,033 3,979 3,902 Net Income 1,788 1,837 1,861 15,274 Earnings Per Common Share (Diluted) .37 .38 .38 3.10 -15- EXTRAORDINARY ITEMITEMS - ------------------------------------- In 4Q 2003,2004, UTMD recognized $500 in extraordinary operating expenses resulting from increasing the Company's reserve for litigation expenses in anticipation of costs to complete the litigation process with the FDA through June 2005. The reduction in accrued income taxes due to the expense was $204, resulting in a $296 decrease to 2004 net income. In 1Q 2004, UTMD recognized extraordinary non-operating income of $6,060 from settlement of additional damages following $24,884 from damages recognized in 4Q 2003 which had been awarded and upheld on appeal as a result offrom a patent infringement lawsuit with Tyco International. Associated with thisthe extraordinary non-operating income from patent infringement damages were G&A Expenses (included in Operating Expenses) of $2,208.$350 in 1Q 2004 and $2,208 in 4Q 2003. These expenses were due to bonuses and additional litigation expenses. The impact ofAccrued income tax on the extraordinary event on UTMD's 12-31-03 Balance Sheetnon-operating income was $24,884$2,361 in receivables (Current Assets)1Q 2004 and $11,458$9,250 in accrued liabilities (Current Liabilities) resulting from accrued income taxes, litigation expense reserve and management bonuses. In addition, year- end Shareholders' Equity was $13,426 higher than would otherwise have been the case without the extraordinary event.4Q 2003. In the following tables, financial data on the previous page have been adjusted to eliminate the extraordinary items. Year Ended December 31 (adjusted) --------------------------------- 2004 2003 2002 2001 2000 ---- ---- ---- ---- ---- Net Sales $26,485 $27,137 $27,361 $26,954 $27,193 Net Income 7,166 7,335 7,165 5,934 5,373 Earnings Per Common Share - (Diluted) 1.53 1.50 1.36 1.14 .90 Quarterly dataData for 2002 is not included below since there is no adjustment applicable to 2002.
Year Ended December 31 (adjusted) --------------------------------- 2003 2002 2001 2000 1999 ---- ---- ---- ---- ---- Net Sales $27,137 $27,361 $26,954 $27,193 $29,444 Net Income 7,335 7,165 5,934 5,373 5,468 Earnings Per Common Share - (Diluted) 1.50 1.36 1.14 .90 .76 Total Assets 24,810 23,387 23,572 25,423 27,756 Working Capital 7,979 5,437 5,400 5,418 5,877 Long-term Debt 0 4,956 2,501 10,000 5,934 Cash Dividends Per Common Share None None None None None Quarterly Data for 2003 (adjusted) ---------------------------------- First Quarter Second Quarter Third Quarter Fourth Quarter ------------- -------------- ------------- --------------2004 (adjusted) ---------------------------------- First Second Third Fourth Quarter Quarter Quarter Quarter ------- ------- ------- ------- Net Sales $6,616 $6,827 $6,670 $6,372 Gross Profit 3,850 3,934 3,779 3,503 Net Income 1,826 1,841 1,807 1,693 Earnings Per Common Share - (Diluted) .38 .38 .39 .39 Quarterly Data for 2003 (adjusted) ---------------------------------- First Second Third Fourth Quarter Quarter Quarter Quarter ------- ------- ------- ------- Net Sales $6,877 $6,840 $6,761 $6,659 Gross Profit 3,977 4,033 3,979 3,902 Net Income 1,788 1,837 1,861 1,848 Earnings Per Common Share - (Diluted) .37 .38 .38 .38
15-16- ITEM 7 - MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS.OPERATIONS The following comments should be read in conjunction with accompanying financial statements. Dollar amounts are in thousands except per-share amounts and where noted. In management's opinion, the extraordinarilyunfavorable extraordinary event in 4Q 2004 of increasing the Company's litigation reserve and the favorable eventextraordinary events in 1Q 2004 and 4Q 2003 of recognizing the Tyco patent infringement damages award hashave an impact on the financialincome statements that does not allow a meaningful comparison of financial ratios and other financial measures with prior periods. Consequently, Item 7 (MD&A) adjusts out the following items related to the extraordinary event,events, prior to making comparisons: BALANCE SHEET adjustment - ------------- ---------- Litigation receivable (24,884) Total current assets (24,884) Total assets (24,884) Accrued expenses - Income taxes payable (9,250) Accrued expenses - Reserve for litigation costs (1,337) Accrued expenses - Payroll and payroll taxes (871) Total current liabilities (11,458) Total liabilities (11,458) Stockholders' Equity (13,426) INCOME STATEMENT - ---------------- Extraordinary item - after tax gain from litigation (13,426) [for year ended 12/31/03] Extraordinary items - (3,054) [for year ended 12/31/04] Note: Income statement comparisons which follow, including earnings per share, are "beforeComparison of balance sheet items and ROE do include the extraordinary item". CASH FLOW STATEMENT adjustment - ------------------- ---------- Net income (13,426) Litigation receivable 24,884 Accrued expenses (11,458)items. -- Productivity of Assets and Working Capital. a) Assets. Year-end 20032004 total assets (adjusted per above) were $24,810,$41,262, compared to $23,387$49,694 in 2002. Because2003. Year-end assets in both years were substantially higher than in prior years due to the extraordinary Tyco patent infringement damages, reflected in cash and investments in year-end 2004 and receivables in year-end 2003. The change in total assets increased whilewas not related to sales were slightly lower relativeactivity. It reflected the difference in the Tyco damages due UTMD at the end of 2003 and the cash and investment balances resulting from the damages at the end of 2004 after income taxes on the extraordinary income had been paid. The same statement applies to 2002, UTMD'sthe net change in current assets. In 2005, total asset turns decreased from 1.2 to 1.1. Ending 2003 current assetswill depend primarily on UTMD's use of $9,018 were higher than 2002 ending current assets of $7,757 primarily because the elimination of the line of credit balance in 3Q 2003 allowed aits cash and investments build-up in 4Q of about $1,200 compared to the end of 2002, whileinvestment balances. Although other current asset categories netted out to remain about the same. Endingsame, 2004 ending inventory balances were about $400 lower and receivables were about $200 higher and ending inventory was about $200 lower. Net property and equipment (PP&E) increased $114 because of the net increase in dollar-valued Ireland PP&E compared to the end of 2002 of about $750, representing about$400 higher. As a 20% change in the U.S. Dollar (USD)/EURO conversion rate. 2003 total PP&E depreciation of $910 exceeded new purchases of $272. Net intangible assets increased $47 because amortization was offset by $121 in new intellectual property investment. After the 2002 adoption of FASB Rule No. 142, UTMD suspended amortizing goodwill from previous acquisitions. Year-ending 2003 net intangible assets were 27% of total assets, compared to 29% at year end 2002. In 2004, asset turns will decrease because of continued cash build-up, unless UTMD makes a substantial acquisition, repurchases stock or takes some other action that consumes cash. Depreciation of fixed assets should continue to exceed new purchases. Net intangible assets may change as the result, of an acquisition or a determination that current goodwill is impaired, although the latter seems unlikely at this time. 2004 total asset turns will depend primarily upon what management can achieve in utilizing excess cash balances. 16 Except for the Oregon facility involved as part of the 1997 CMI acquisition and a portion of UTMD's Midvale parking lot, the Company owns its PP&E assets. PP&E assets are comprised of Utah and Ireland manufacturing facilities, molds, production tooling and equipment, test equipment, computer/ communications equipment and software. Net PP&E in the U.S. decreased $508 due to depreciation in excess of purchases. In Ireland, PP&E increased $622, despite no significant new asset purchases and depreciation expense of $153 because of the weaker USD. With slightly lower consolidated sales and higher PP&E in USD terms, 2003 PP&E turns decreased to 3.0 from 3.1. The current book value of consolidated PP&E is 38% of acquisition cost. Management believes that PP&E is in good working order and capable of supporting increased sales activity. Going forward, financial performance should be enhanced by lower rates of depreciation and continuing higher PP&E turns. The goodwill on UTMD's balance sheet is the result of two acquisitions in 1997 and 1998 which were made in cash at conservative valuations. As of December 31, 2003, the goodwill on the balance sheet has been reduced by 27% from the acquisition price as a result of UTMD using previous GAAP through 2001 for the purchase method of acquisition accounting. UTMD's future income statement performance could be affected in the case of impairment of the existing goodwill. The acquired 1998 Gesco neonatal products and 1997 CMI products continue to be viable parts of UTMD's overall business activities, representing 22% of total sales in 2003. Net goodwill on the December 31, 2003 balance sheet is 23% of 2003 sales. UTMD does not expect its goodwill intangible assets to become impaired in the foreseeable future. Average inventory turns decreased in 2003 to 3.3 from 3.4 because average inventory balances remained about the same as 2002 while sales declined slightly. The 2003 ending inventory balance was about $100 below the year's average. Management continues to target 4.0 average inventory turns as its objective, and believesincreased to 3.7 in 2004 from 3.3 in 2003 despite a decline in sales activity. Management expects to sustain 3.7 inventory turns will improve in 2004. Year-ending 20032005. Because year-ending 2004 accounts receivable (A/R) balances increased 8%. Calculated12%, calculated average days in A/R were 45aging was 51 on December 31, 20032004 based on 4Q 20032004 shipment activity. ThisAlthough this is well within management's objective of 55 days.days, it is less favorable than at the end of 2003. A/R over 90 days from invoice date were about 4%5% of total A/R at year end,year-end 2004, compared to 7%4% at year-end 2002.2003. The Company believes these older A/R are collectible or within its reserve balances for uncollectible accounts. Working capital at year-end 20032004 was $7,979$20,194 compared to $5,437$21,405 at year-end 2002 because in addition2003. Both amounts far exceed UTMD's working capital needs for normal operations. UTMD's current ratio increased to 5.7 from 2.7, due mainly to the increasedecrease in cash and investment balances of about $1,200, current liabilities atincome taxes due resulting from the end of the year were about $1,300 lower. As a result, UTMD's Current Ratio improved to 8.7 from 3.3. 2004extraordinary items. 2005 working capital balances and current ratio will depend primarily upon the timing and extent of management'suse of cash and investment balances. The non-cash and investment components of working capital are expected utilizationto remain within management targets. Property, plant and equipment (PP&E) assets are comprised of excess cash.Utah, Oregon and Ireland manufacturing molds, production tooling and equipment, test equipment, computer/ communications equipment and software, and the Utah and Ireland facilities. UTMD leases the Oregon facility, involved in the 1997 CMI acquisition, and a portion of the Midvale parking lot. In 2004, PP&E depreciation of $739 exceeded new PP&E asset purchases of $411. Net PP&E assets, however, increased $53 compared to the end of 2003 because of a $252 increase in dollar-valued Ireland PP&E assets. In 2004, the U.S. dollar (USD) declined in value relative to the euro by about 8%. Slightly higher consolidated PP&E (in U.S. dollar terms) and lower sales resulted in a slightly lower PP&E turn. In 2005, depreciation of fixed assets is expected to exceed new fixed asset purchases required to sustain current operations, which will improve PP&E asset turns unless the U.S. dollar continues to weaken, further inflating the dollar value of Ireland PP&E. The current book value of consolidated PP&E is 37% of acquisition cost. Management believes that PP&E is in good working order and capable of supporting increased sales activity. -17- Intangible assets are comprised of goodwill resulting from acquisitions and the costs of obtaining patents and other technology rights. Net intangible assets (NIA) increased to $7,674 at the end of 2004 from $6,787 at the end of 2003. The $7,191 goodwill portion of NIA at the end of 2004 is the result of three acquisitions in 1997, 1998 and 2004 which were made in cash at conservative valuations. Goodwill increased $946 in 2004 as a result of the acquisition of Abcorp Medical, UTMD's supplier of fetal monitoring belts. The increase in 2004 goodwill was offset by $70 amortization of other intangible assets. As of the end of 2004, goodwill on the balance sheet has been reduced by 24% from the goodwill resulting at time of acquisition. The reduction is a result of UTMD using previous GAAP through 2001 for the purchase method of acquisition accounting. Under current GAAP, the goodwill will not be amortized as an expense unless and until the value of the acquired entity becomes impaired. The acquisitions reflected in goodwill continue to be viable parts of UTMD's overall business activities, representing 26% of total sales in 2004. UTMD does not expect its goodwill intangible assets to become impaired in the foreseeable future. b) Liabilities. In the years 2002-2003,Excluding accrued and deferred income taxes, UTMD's total liabilities at the end of 2004 and 2003, which were $3,952 and $3,227, respectively, were both less than 10% of total debt ratio have been drivenassets reduced by the timing of debt incurred for financing share repurchases, not in providing cash to operate its business.total accrued tax liability. At the end of 2003,2004, UTMD's total debt ratio decreased to 7%12% from 33%26% at the end of 2002 primarily because the line-of-credit balance2003. The decline was paid off. In 3Q 2003, UTMD retired the debt associated with its November 2002 tender offer under which it repurchased 503 thousand shares at a cost of $8.6 million. Total shares repurchased in 2002 including the tender offer were 721 thousand at a cost of $11.8 million. In 2003, in addition to eliminating the debt balance from financing the 2002 share repurchases, UTMD repurchased 97 thousand shares in the open market at a cost of $2.2 million. UTMD's total debt ratio in 2004 will depend on any financing required to continue to repurchase shares or make acquisitions. Without requirement for any of those financing activities, the total debt ratio due to normal current liabilities should beaccrued taxes on the extraordinary item on the balance sheet at the end of 2003 which were paid in the range of 10%.2004. Results of Operations. a) Revenues. Global consolidated sales decreased about 1%2% in 20032004 compared to 2002.2003. Foreign (international) sales increased 2% and3% while U.S. (domestic) sales declined 2%4%. 17 Revenues were negatively affected by an August 10 FDA press release that announced that the FDA filed a lawsuit against UTMD. International revenues continued to be negatively affected by the FDA's refusal, continuing since 2003, to provide Certificates to Foreign Governments (CFGs). UTMD divides its domestic sales into two primary distribution channels: "direct sales" which are sales to end user customers by UTMD's direct sales force, independent commissioned sales reps, specialty distributors and national hospital distribution companies, and "OEM sales" which are component sales to other companies where products are packaged and resold as part of another company's product offerings. As a percentage of total domestic sales, 2003 direct sales representedwere 93% compared toof domestic sales in both 2004 and 2003, and 94% in 2002 and 92% in 2001.2002. The remaining sales were OEM sales, e.g. 7% of domestic sales in 20032004 were domestic OEM sales. Domestic direct sales represented 73%72% of global consolidated sales in 20032004 compared to 73% in 2003 and 74% in both 20022002. Domestic direct sales which appeared least affected by the FDA announcement were sales where clinicians make the purchase decision. Consequently, the least affected sales were sales to physician offices and 2001.clinics. Hospital labor and delivery (L&D) department sales appeared to be the most affected. Hospital NICU sales were less affected than L&D because practitioners still have major discretion in determining what products are purchased. In order to help gain further attention of concerned hospital administrators, UTMD instituted a special "loyalty discount" in late August. Ignoring the effect of the special U.S. hospital customer loyalty discount (the Discount) in effect from August 20 through November 30, 2004, UTMD's sales were down 1% from 2003. The amount of the Discount was $374. International sales in 20032004 were 22%23% of global consolidated sales compared to 21%22% and 19%21% in years 2003 and 2002, and 2001 respectively. InOf the first half of the year,2004 international sales, had increased 12% primarily helped by a weaker U.S. Dollar. In the second half, a decision by the FDA to withhold export certificates from UTMD probably contributed to an international sales decline of 6%. Of the 2003 foreign sales, 58%60% were made in Europe, the same ascompared to 58% in both 20022003 and 2001.2002. Ireland operations (UTMD Ltd.) shipped 63%59% of international sales (in USD terms) in 20032004 compared to 63% in 2003 and 59% in 2002 and 54% in 2001. Shipments,2002. UTMD Ltd. 2004 shipments, including intercompany from UTMD Ltd. (Ireland)to Midvale, were down 2%15% in Euroeuro terms, and up 16%down 5% in USD terms, compared to the prior year.2003. UTMD groups its sales into four product-line categories: 1) obstetrics, comprised of labor and delivery management tools for monitoring fetal and maternal well-being, for reducing risk in performing difficult delivery procedures and for improving clinician safety; 2) gynecology/ electrosurgery/ urology, comprised of tools for gynecological procedures associated primarily with cervical/ uterine disease including LETZ, endometrial sampling, diagnostic laparoscopy, and other MIS procedures; specialty excision and incision tools; -18- conservative urinary incontinence therapy devices; and urology tools; 3) neonatal care, comprised of devices that provide developmentally-friendly care to the most critically ill babies including providing vascular access, administering vital fluids, maintaining a neutral thermal environment, providing protection and assisting in specialized applications; and 4) blood pressure monitoring/ accessories/ other, comprised of specialized components for invasively monitoring blood pressure on a continuous basis with pressure transducer systems, and subcontract molded parts along with other components and products sold on an OEM basis to other companies. In these four categories, UTMD's primary revenue contributors often enjoy a dominant market share and typically have differentiated product features protected by patents. Revenues by product category: 1. Worldwide obstetrics product sales were $10,918 in 2004 compared to $11,435 in 2003 compared toand $11,977 in 2002 and $12,276 in 2001.2002. Without the Discount, 2004 obstetrics sales were $11,120. Of the $542$517 decline in total obstetrics sales, $252$154 was from lower sales of vacuum-assisted delivery systems (VADS), a 15%an 11% decline, and $237$1,136 from lower Intran Plus (IUPC) sales, a 2%12% decline. TheAbcorp sales of $842 helped offset the declines. After August 10, the lower IUPC and VADS sales resulted primarily from concerns of hospital administrators related to the press release from the FDA. Other contributing factors included a changetrend in obstetrics practice that favors abdominal operative deliveries over vaginal operative deliveries because of medical malpractice litigation risk. Lower obstetrics sales in general resulted fromrisk, and increased competition including effects of product bundling agreements with U.S. hospital administrators. Despite the decline in utilization, UTMD agrees with ACOG (The American College of Obstetricians & Gynecologists) that using VADS remains the trained physician's best choice in many operative deliveries, and will continue its educational programs regarding appropriate indications and proper use of the procedure.agreements. Cheaper priced, less clinically-effective products represent significant competition where hospital administrators are constrained by GPO contracts or may not take the total cost of care into consideration, including increased risk of complications and utilization rates. International obstetrics sales increased to $774 in 2004 from $665 in 2003 from $613 in 2002.2003. 2. Consolidated global gynecology/ electrosurgery/ urology product sales were $5,142 in 2004 compared to $5,324 in 2003 compared toand $5,271 in 2002 and $4,924 in 2001.2002. Without the Discount, 2004 sales were $5,212. International sales in this category increased 19%decreased 9%. A number of UTMD products in this fragmented category are patented, soInternational sales should continuewere negatively affected by not being able to grow as physicians learn more about their advantages. 18 supply requested FDA CFGs to international distributors. 3. Consolidated global neonatal product sales were $4,134 in 2004 compared to $4,142 in 2003 compared toand $3,852 in 2002 and $3,801 in 2001.2002. Without the Discount, 2004 sales were $4,217. International neonatal product sales decreased 16%increased 39%. 4. Worldwide blood pressure monitoring and accessories (BPM) sales were $6,292 in 2004 compared to $6,236 in 2003 compared toand $6,261 in 2002 and $5,953 in 2001. Domestic OEM2002. Without the Discount, 2004 sales were $6,310. International sales in this category, which includes plastic molded components used in other industries affected by the weak U.S. economy, increased 2%. Looking forward to 2004, UTMD expects2005, UTMD's improvement in sales depends primarily on the timing of a favorable resolution of the lawsuit with the FDA, receipt of CFGs and restoration of its good reputation for supplying high quality devices. If the FDA lawsuit is resolved by the middle of the year, management believes that it can achieve a 2-3% increase in 2005 sales relative to maintain or modestly increase sales for its established products even though markets for its products will remain intensely competitive; despite the fact that administrative barriers in the U.S. that prevent smaller companies from fairly competing for hospital sales have not been significantly diminished; and despite disappointment in U.S. FDA administrators who we believe have inappropriately withheld export certificates to foreign governments since 2003.2004. b) Gross Profit. UTMD's average 20032004 gross profit margin (GPM), the surplus after costs of manufacturing, inspecting, packaging, sterilizing and shipping products (COGS) are subtracted from net revenues, was 56.9% compared to a Company record 58.6% compared toin 2003 and 57.6% in 20022002. As a percentage of sales, the negative effect of the Discount was more pronounced on gross profits than on sales. In 2004, UTMD experienced higher materials costs, particularly for plastics, along with increased labor costs, lower absorption of fixed overhead costs because of lower sales, and 57.1% in 2001. UTMD continued to experience a favorablean unfavorable shift from lowerhigher margin products to higherlower margin products as a percentage of sales,products. The unfavorable cost trends were partially offset by lower depreciation expense on fixed assets and improved efficienciesrecoveries of previous years' misappropriated funds. With regard to the latter, UTMD recognized a favorable contribution to gross profit of $180,830 and $241,670 for 4Q 2004 and 2004, respectively, as the result of recovery of misappropriated funds that had reduced gross profit performance in overhead costs.prior years. The Audit Committee of UTMD was fully involved in the investigation and resolution of this matter. With respect to gross profits in UTMD's sales channels, OEM sales are sales of UTMD productscomponents that are marketed by other companies in conjunction withas part of their product offerings, and are not sold under UTMD's label.offerings. UTMD utilizes "OEM sales"OEM sales as a means to help maximize utilization of its capabilities established to satisfy its "direct sales"direct sales business. As a general rule, prices for "OEM product sales"OEM sales expressed as a multiple of direct variable manufacturing expenses are lower than for "direct sales"direct sales because, in the OEM and international channels, UTMD's business partners incur significant expenses of sales and marketing. Because of UTMD's small size and period-to-period fluctuations in OEM business activity, allocations of fixed manufacturing -19- overheads cannot be meaningfully allocated between direct and OEM sales. Therefore, UTMD does not report GPM by sales channels. UTMD targets an average GPM greater than or equal to 55%, which it believes is necessary to successfully support the significant operating expenses required in a highly complex and competitive medical device marketplace. Management expects to achieve itsthis GPM target again in 2004.2005. Expected favorable influences include growth in sales volume without a similar increase in manufacturing overhead expenses, a larger percentage of total sales from higher margin products and a continued emphasis on reengineering products and processes to reduce costs. Expected unfavorable influences are continued increases in material costs, competitive pressure on pricing and higher wage rates. c) Operating Profit. Operating profit, or income from operations, is the surplus after operating expenses are subtracted from gross profits. Operating expenses include sales and marketing (S&M) expenses, research and development (R&D) expenses and general and administrative (G&A) expenses. 2003Operating expenses in 2004 were lower by $214 than in 2003. However, because of lower gross profits, 2004 operating profit increased 2%decreased 6% to $10,109 compared to $10,722 compared to $10,542 in 2003. 2002 and $9,278 in 2001.operating profits were $10,542. UTMD's operating profit margin (operating profits divided by total sales) was also a Company record38.2% in 2003. The 2003 operating profit margin of 39.5%2004, compared to a record 39.5% in 2003 and 38.5% in 2002 and 34.4% in 2001.2002. Operating expenses as a percentage of sales were 18.7% in 2004, compared to 19.1% in both 2003 and 2002, compared to 22.7% in 2001. A major portion of the decrease in 2002 from 2001 was due to UTMD's required GAAP adoption of SFAS Statement No. 142, under which the Company recognized no goodwill amortization expense (GWA) in 2003 or 2002. GWA was $569 in 2001. For comparison, $569 represents 2.1% of 2003 and 2002 sales. Looking forward to 2004,2005, UTMD expects to continue to achieve an outstanding operating margin similar to 2003, primarily as a result of an increase in sales coupled with holdingby maintaining its GPM above 55% and controlling operating expenses aboutbelow 19% of sales. The primary risk to achieving that expectation is a delay in the same. In orderexpected resolution of the lawsuit with the FDA. A further delay would be a double negative by continuing to hold operating expensesretard sales activity while at the same UTMD expects to be able to offset an increase in S&M expenses with a decrease intime increasing litigation expenses (G&A expenses). 19 costs which are time-related. i) S&M expenses: S&M expenses are the costs of communicating UTMD's differences and product advantages, providing training and other customer service in support of the use of UTMD's solutions, processing orders and funding GPO fees. Because UTMD sells internationally through third party distributors, its S&M expenses are predominantly neededemployed for U.S. business activity where it sells directly to clinical users. The largest component of S&M expenses is the cost of directly employing representatives that provide coverage across the U.S. Year 20032004 S&M expenses decreased to $2,253 from $2,364 fromin 2003 and $2,472 in 2002, and $2,773 in 2001, as UTMD continued to improvefocus on the productivity of its direct sales force. As a percent of total sales, S&M operating expenses were 8.5% in 2004, 8.7% in 2003 and 9.0% in 2002 and 10.3% in 2001.2002. Looking forward, UTMD plans higher S&M expenses during 20042005 due to Group Purchasing Organization fees, increased advertising expenses and new marketing initiatives, but intends to manage S&M expenses to remain less than 10%9% of total sales. ii) R&D expenses: R&D expenses include the costs of investigating clinical needs, developing innovative concepts, testing concepts for viability, validating methods of manufacture, completing regulatory documentation and other activities required for design control, responding to customer requests for product enhancements, and assisting manufacturing engineering on an ongoing basis in developing new processes or improving existing processes. Internal R&D expenses were $292 in 2004, $288 in 2003 and $285 in 2002 and $364 in 2001.2002. As a percent of sales, 20032004 and 20022003 R&D expenses were 1.0%1.1% compared to 1.3%1.0% in 2001. In 2003, the efforts of R&D aided UTMD's continued GPM improvements.2002. In addition to new products still being developed, a number of existing products were enhanced or updated.updated in 2004. In 2004,2005, UTMD will opportunistically employ R&D resources to invest where management anticipates it can get a significant return with future new product sales. 20042005 R&D expenses are again likely to be in the range of 1%-2% of sales. iii) G&A expenses: G&A expenses include the "front office" functional costs of executive management, finance and accounting, corporate information systems, human resources, shareholder relations, legal, risk management and protection of intellectual property. In addition to employing the personnel required to coordinate or manage the preceding functions, G&A expenses include outside director costs, outside legal counsel, independent accounting audit fees, 401(k) administration, NASDAQ exchange fees, write-offs of uncollectible receivables, business insurance costs and corporate contributions to charitable organizations. Prior to 2002, G&A expenses also included GWA. G&A expenses were $2,412 in 2004, $2,517 in 2003 and $2,464 in 2002 and $2,978 in 2001.2002. As a percent of sales, G&A expenses were 9.1% in 2004, 9.3% in 2003 and 9.0% in 2002 and 11.1% in 2001.2002. All three years included considerable litigation expenses relating to the patent infringement lawsuit with Tyco/Kendallo LTP.KendalloLTP or lawsuits with the FDA. In addition, 2002 and 2003all three years include increasedincreasing G&A expenses to comply with -20- required governance activities mandated by theThe Sarbanes Oxley Act of 2002. It is management's objective to hold G&A expenses to about 9% of sales again in 2005. d) Non-operating Income, Non-operating Expense and EBT. Non-operating income includes royalties from licensing UTMD's technology to other companies, rent from leasing unutilizedunderutilized property to others, interestincome earned from investing the Company's excess cash and gains or losses from the sale of assets, offset by non-operating expenses which includesinclude interest expenses and bank fees. Non-operating income was $798 in 2004, $454 in 2003 and $453 in 20022002. The increase in 2004 resulted from investment income on much higher average cash and $202 in 2001.investment balances, higher rental income and no interest expense. Royalties received were $450 in all three years. Future royalties may vary depending on the success of other companies in selling products licensed by UTMD, and the remaining life of the applicable patents. InterestIn 2004, UTMD had no interest expense associated with the line-of-credit which reduced non-operating income was $47 in 2003, $36 in 2002 and $370 in 2001. Interest costs inbecause it did not utilize its bank line-of-credit. In 2003 and 2002, were lower compared to 2001 because of significantly lower average LOC debt balances,respectively, interest expense was $47 and because interest rates were lower after 2001.$36. UTMD expects non-operating income in 20042005 to be higher than 2003 because of interest income on excess cash balances, but thisbetween $500 and $800. The actual amount received will depend on many factors including: the timing of utilization of cash balances for share repurchases, dividends or acquisitions; the excessmarket performance of UTMD's liquid investments; the need for capital to support litigation; and cash as well as prevailing interest rates.flow from normal operating performance. Earnings before income taxes (EBT) result from adding UTMD's non-operating income to its operating profits. EBT were $10,907 in 2004, $11,176 in 2003 and $10,996 in 2002 and $9,480 in 2001.2002. EBT in 20032004 were 2% higherlower than in 2002 although sales were 1% lower because of record gross profit margins.2003, the same percentage decrease as sales. Given the 2005 projections previously noted, above, management is targeting 20042005 EBT of about the same as 2003 EBT (excluding the extraordinary non-operating income and operating expenses associated with the Tyco patent infringement lawsuit). 20 $11,000. e) Net Income, EPS and ROE. Net income is EBT minus income taxes. Net income increasedin 2004 decreased 2%, consistent with the change in sales, to $7,166 from $7,335 in 2003 from $7,165 in 2002. 20012003. 2002 net income was $5,934.$7,165. The growth rate in Net Income was slightly higher than EBT because UTMD's 2003 effective tax rate was lower than in 2002. The (adjusted) effective income tax rate in 20032004 was 34.4%34.3% compared to 34.4% in 2003 and 34.8% in 2002 and 37.4% in 2001.2002. Tax on the extraordinary itemitems was 40.8%41.4%, resulting in a combined tax rate of 38.7%36.6%. Year to year fluctuations in the tax rate have resulted fromfrom: 1) the use of a foreign sales corporation, 2) differences in distribution of state income taxes, 3) differencestaxes; 2) variations in profits of the Ireland subsidiary which is taxed at a 10% rate on exported manufactured products,products; 3) extraterritorial income exclusions; 4) increases inhigher marginal tax rates for EBT above $10 million,million; and 5) other factors such as R&D tax credits and the timing of actual versus accrued litigation expenses. The Company eliminated its foreign sales corporation in 2002.credits. Management expects that UTMD's consolidated income tax rate mayshould be highersimilar in 20042005 compared to 2003,2004, but this is difficult to predict. UTMD's normal net income expressed as a percentage of sales ranks in the top performance tier of all U.S. publicly-traded companies at 27.0%27.1%, 26.2%27.0% and 22.0%26.2% for years 2004, 2003 2002 and 2001,2002, respectively. This profitability performance factor is the primary driver for UTMD's return on shareholders' equity (ROE). Earnings per share (EPS) is net income divided by the number of shares of stock outstanding (diluted to take into consideration stock option awards which are "in the money" -money," i.e., have exercise prices below the current period's weighted average market value). Diluted 20032004 EPS were $1.53, up 2% from $1.50 up 10% from $1.36 in 2002.2003. In 2001,2002, EPS were $1.14 with sales about the same as 2003. The combination of higher profitability and fewer$1.36. Fewer outstanding shares accounted for the substantial increase in EPS. UTMD management believes shareholder value is improved by consistently increasing EPS. InOver the last six year periodseven years since 1997, UTMD has increased EPS at an annually compounded rate of 20%17% per year. The end of 20032004 weighted average number of diluted common shares (the number used to calculate diluted EPS) were 4,8854,675 (in thousands) compared to 4,885 shares in 2003 and 5,263 shares in 2002 and 5,210 shares in 2001.2002. Dilution for "in the money" unexercised options for the year 20032004 was 359276 (in thousands) shares compared to 359 in 2003 and 350 in 2002, and 191 in 2001.2002. The total number of unexercised options outstanding declinedat year-end was about 23%the same in 2004 as 2003, following a 9%23% decline in the prior year. Dilution has increased despite much fewerdecreased in 2004 from 2003 because the average number of options outstanding option shares due to UTMD'sdecreased substantially, partially offset by a higher average share price in the stock market. Actual outstanding common shares as of December 31, 20032004 were 4,544,000.4,105,000. Return on shareholders' equity (ROE) is the portion of net income retained by UTMD (after payment of dividends) to internally finance its growth, divided by the average accumulated shareholders' equity during the applicable time period. Because ROE includes balance sheet measures as well as income statement measures, the calculations of ROE which follow do not exclude the extraordinary items. ROE in 20032004 was 38%23% (28% before dividends), compared to 79% in 2003 and 42% in 2002 and 39% in 2001.2002. This ratio determines how fast the Company can afford to grow -21- without adding external financing that would dilute shareholder interests. For example, a 20% ROE will financially support 20% growth in revenues without issuing more stock. Record profitabilityThe lower ROE in 2004, despite a continued excellent net profit margin, was primarily responsible fordue to payment of dividends to shareholders which reduced retained profits, much higher average cash and investment balances which reduced total asset turns, and no long-term debt which reduced financial leverage compared to prior years. Looking forward, 2005 ROE is projected to be lower than 2004 if cash and investment balances are maintained at current levels, shareholder dividends are continued outstanding ROE result in 2003.and no other extraordinary income is received. In UTMD's opinion, achieving growth in revenues and EPS without diluting shareholder interests maximizes shareholders'shareholder value. Management's goal is to consistently achieve ROE in excess of 25%. UTMD's ROE has averaged 31%34% per year over the last 18 years. Although the accumulation of cash in the absence of share repurchases or acquisitions could reduce total asset turns, and the elimination of long term debt would reduce financial leverage that enhances ROE, management expects to be able to achieve its ROE objective again in 2004 primarily by accomplishing another record year in profitability, assuming UTMD effectively deploys its excess cash resulting from the extraordinary event. Liquidity and Capital Resources. Cash flows.Flows. Cash (and investment) balances were $16,928 at the end of 2004, compared to $1,484 at the end of 2003, compared to $285 at the end of 2002. 21 2003. Net cash provided by operating activities, including adjustments for depreciation and other non-cash operating expenses, along with changes in working capital, totaled $27,459 in 2004 compared to $8,335 in 2003 compared toand $8,656 in 20022002. Major changes in operating assets and $7,860liabilities in 2001.both 2004 and 2003 were related to the accrual and receipt of about $31 million from Tyco International for patent infringement, and taxes on that income. Cash provided by operating activities demonstrates the company'sin 2004 includes continued control of operatingexcellent net income performance, aided by a $1,108$446 tax benefit attributable to exercise of employee options, in 2003, compared to the same tax benefit in 20022003 of $1,108 and $354 and in 2001 of $60.2002. The increase in the Company's use of cash for investing activities was fromprimarily as a result of purchases of short termshort-term investments, in an effort to make prudent use of excess cash. The Company realized $41UTMD expended $22,103 in gains from the sale of investments.2004 on such purchases, compared to $737 in 2003 and none in 2002. In 2003,2004, UTMD received $882$8,202 from selling short-term investments. UTMD invested $1,012 in second quarter 2004 to acquire Abcorp, Inc., its vendor for fetal monitoring belts. Please see the table under Supplemental Disclosure of Cash Flow Information for detail of the Abcorp assets purchased. In 2004, UTMD received $1,111 and issued 197,432117,482 shares of stock upon the exercise of employee and director stock options. Employees and directors exercised a total of 298,852122,908 option shares in 2003,2004, with 101,4205,426 shares immediately being retired as a result of the individuals trading the shares in payment of the exercise price of the options and relatedoptions. UTMD paid $6 to meet tax withholding requirements. UTMD paid $555 to meet those tax withholding requirements.requirements on options exercised. UTMD repurchased 96,900555,765 shares of stock in the open market at a cost of $2,240$10,692 during 2003.2004. Option exercises in 20032004 were at an average price of $8.26$10.05 per share. Share repurchases in the open market were at an average cost of $23.12$19.24 per share, including commissions and fees. In 2002,2003, the Company received a net $1,082$882 from issuing 135,362197,432 shares of stock on the exercise of employee and director stock options, including 1,727101,420 shares retired upon an employee trading those shares in payment of the stock option exercise price.price and related tax withholding requirements. During 2004, UTMD did not utilize its bank line of credit. In 2003, UTMD made repayments of $4,956 on its note payable, which waseliminated the line of credit balance remaining balance at the end of 2002, while receiving $0 in proceeds from the note (lineline of credit).credit. In 2002, UTMD made loan repayments of $2,501 and received $4,956 in proceeds from the noteline of credit to finance the November 2002 tender offer. The 2002 loan proceeds were used to payoffer for UTMD share repurchases as the result of a tender offer.repurchases. Management believes that future income from operations and effective management of working capital will provide the liquidity needed to finance growth plans. Planned 20042005 capital expenditures are expected to be approximately $600 to keep facilities, equipment and tooling in good working order. In addition to capital expenditures, UTMD plans to use cash in 20042005 for selective infusions of technological, marketing or product manufacturing rights to broaden the Company's product offerings; for continued share repurchases if the price of the stock remains undervalued; and if available for a reasonable price, acquisitions that may strategically fit UTMD's business and are accretive to performance. The revolving line of credit line will continue to be available for liquidity when the timing of acquisitions or repurchases of stock require a large amount of cash in a short period of time in excess ofnot otherwise available from existing cash and investment balances. Management-22- In summary, management plans to use theutilize cash from the Tyco damagesnot needed to support normal operations in one or a combination of the following: 1) to make investments in new technology,technology; 2) to acquire a product line that will help spur revenue growth and better utilize UTMDs infrastructure,UTMD's infrastructure; and/or 3) to buy back UTMD shares in the open marketplace. [Remainder of Page Intentionally Left Blank] 22 Contractual Obligations and Contingent Liabilities and Commitments The following is a summary of UTMD's significant contractual obligations and commitments as of December 31, 20032004 (in thousands): Less More Contractual Obligations and Less More Commitments than 1 1-3 3-5 than 5 -----------Commitments Total year years years years ------- ------------------ ------ ------ ------ ------ ------ Long-term debt obligations ..... $ --- $ --- $ --- $ --- $ --- Operating lease obligations..... 1,065 66obligations 1,095 108 142 111 111 777734 Purchase obligations (1)........ 2,720 2,720 - - - ------- ------- 1,788 1,788 -- -- -- ------ ------ ------ Total.....................------ ------ Total $2,883 $1,896 $ 3,785 $ 2,786142 $ 111 $ 111 $ 777 ======= =======734 ====== ====== ====== ====== ====== (1) The majority of UTMD's purchase obligations constitute raw materials for use in its manufacturing operations. UTMD has the right to make changes in, among other things, purchase quantities, delivery schedules and order acceptance. Off-Balance Sheet Arrangements UTMD's only off-balance sheet arrangements are 1) an operating leaseslease on its Oregon manufacturing facility, and on2) a lease for a portion of the parking lot adjacent to its Utah facilities.manufacturing facility. Details on those arrangements are provided above, and in Note 6 on page F-17. Other Financial Measures EBITDA (=(equals EBT, plus depreciation and amortization expenses, plus interest expense) is a term used for measuring a company's ability to generate cash from its operations without regard for changes in working capital, cash consumed for fixed asset purchases, its cost of borrowing or income tax burden. UTMD's EBITDA from normal operations in 20032004 was $12.2$11.7 million, or 45%44% as a ratio of sales. UTMD'sIn both 2003 and 2002, EBITDA has averaged 40%was 45% of sales over the last five years.sales. The extraordinarily strong cash generation performance resulted from a combination of outstanding operating profit performance andexcellent profitability together with royalty income from others' use of UTMD's technology. UTMD's 2004 EBITDA including extraordinary items was $16.9 million. With sales and other performance factors approximately the same as in 2003,projected above, management projectsexpects 2005 EBITDA from normal operations to be about the same in 2004.$12 million. Please note that EBITDA is not defined or described by Generally Accepted Accounting Principles (GAAP). As such, it is not prepared in accordance with GAAP, is not a measure of liquidity, and is not a measure of operating results. However, the components of EBITDA are prepared in accordance with GAAP, and UTMD believes that EBITDA is an important measure of the Company's operating performance and financial well-being. Management's Outlook. In summary, in 20042005 UTMD plans to 1) clear up its apparently unresolved QSR status with the U.S. FDA that has hindered international sales, slowed new product development, stymied business development and consumed an inordinate amount of human capital since 2002;2001; 2) continue outstanding operating performance; 3) actively look for new acquisitions to facilitate sales growth; and 4) utilize current excess cash balances in shareholders' best long termlong-term interest. The following factors provide optimism that 2004 will demonstrate better top line growth: 23-23- 1) the continued scrutiny by government agencies into the anti-competition, anti-innovation and anti-good healthcare effects of bundling agreements and exclusive agreements for physician preference products by hospital administrators. 2) recent supply agreements with five of the top seven hospital GPOs. 3) continued improvements in a maturing U.S. direct sales force. 4) improvement in general economic conditions that have negatively affected U.S. OEM activity. 5) elimination of unfavorable regulatory interference affecting export sales. UTMD will continue to focus on differentiating itself, especially from commodity-oriented competitors. UTMD is small, but its employees are experienced and diligent in their work. Our passion is in providing innovative clinical solutions that will help reduce health risks for women and their babies. The Company has a defined focus and does not seek to become big as a primary motivation. We just want to do an excellent job in meeting our customers' needs and provide our shareholders with excellent returns. The reliability and performance of UTMD's products is high and represents significant clinical benefits as well as minimal total cost of care. Physicians do care about the well-being of their patients, but their time is limited to evaluate choices, and they have hospital administrators to deal with who often look at the initial price of a product, without understanding the total picture including complications and other less obvious costs.cost of care picture. In the U.S., UTMD will continue to leverage its reputation as an innovator which will responsively take on challenges to work with physicians who use its products in specialty hospital areas, or outside the hospital in their office practices. Internationally, where UTMD must depend on the knowledge, focus, relationships and energy of independent distributors, management will continue to closely monitor performance and recruit needed new business partners. UTMD's 2004 EPS were up 2%, and its $22.47 2004 ending share price was down 14% relative to the end of 2003. In 2003,comparison, the NASDAQ Composite, S&P 500 Index and DJIA were up, 9%, 9% and 3%, respectively, in 2004. Looking back five years to the end of 1999, UTMD's EPS have more than doubled, and its year-ending share price has more than tripled. In comparison, the NASDAQ Composite, S&P 500 Index and DJIA were down 46%, down 17% and down 6%, respectively, over that same five year time span. In 2004, UTMD again demonstrated a high positive cash flow, reflected by achieving record EBITDA performance of 45% of sales, managing working capital effectively and keeping new capital expenditures below its rate of depreciation of existing assets. UTMD's balance sheet is strong enough to finance an acquisition in 20042005 without issuing stock. In considering acquisitions, UTMD looks to acquire successful companies that will enhance its specialist focus. When UTMD acquires a company, it probably will be for cash and with the idea that it will be able to retain key resources that helped make the acquired entity previously successful. Over the last six years, UTMD has made some significant accomplishments: 1) compounded EPS growth of 20% per year (not including receipt of patent infringement damages); 2) two accretive acquisitions which now represent about 22% of the Company's business activity; 3) repurchase of 45% of the ownership of the Company (including dilution of options) for $36 million (3.7 million net shares at an average cost of $9.75 per share including commissions, other repurchase costs and the difference between option exercise price and market price for option shares exercised); and 4) a successful effort defending the patent rights of UTMD's flagship product technology and core franchise of UTMD's market identity, resulting in a $31 million damages award. Looking back, UTMD's EPS were up 10% in 2003, and the $26.14 ending share price was up 37% relative to the end of 2002. The NASDAQ Composite, S&P 500 Index and DJIA were up, 50%, 29% and 25% respectively in 2003. With 2003 EPS of $1.50 (excluding Tyco damages award), UTMD's year-end price to trailing earnings ratio (PER) was 17, suggesting that a combination of PER expansion closer to the medical device industry average and continued increases in EPS performance could again provide excellent shareholder returns in 2004. Accounting Policy Changes. In May 2003,December 2004, the FASB issued SFAS 150,123 (revised 2004), "Accounting for Certain Financial Instruments with Characteristics of both Liabilities and Equity.Stock Based Compensation." This new statement changessupersedes APB Opinion No. 25, "Accounting for Stock Issued to Employees." This revised statement establishes standards for the accounting of transactions in which an entity exchanges its equity instruments for certain financial instruments that, under 24 previous guidance, issuers could account for as equity or classifications between liabilitiesgoods and equity in a section that has been known as "mezzanine capital." It requires that those certain instruments be classified as liabilities in balance sheets. Mostservices, including the grant of the guidance in SFAS 150 is effective for all financial instruments entered into or modified after May 31, 2003.stock options to employees and directors. The adoption of SFAS 150 did not have any impact on the Company's consolidated financial statements. In April 2003, the FASB issued SFAS 149, "Amendment of Statement 133 on Derivative Instruments and Hedging Activities." SFAS 149 amends and clarifies financial accounting and reporting for derivative instruments, including certain derivative instruments embedded in other contracts (collectively referred to as derivatives) and for hedging activities under SFAS 133, "Accounting for Derivative Instruments and Hedging Activities". This Statement is effective for contracts entered into or modified after June 30, 2003, with certain exceptions, and for hedging relationships designated after June 30, 2003, with certain exceptions. The adoption of SFAS 149 did not have any effect on the Company's consolidated financial statements. In January 2003, the FASB issued Interpretation 46, "Consolidation of Variable Interest Entities" (FIN 46), which addresses consolidation by business enterprises of variable interest entities. FIN 46 clarifies the application of Accounting Research Bulletin No. 51, "Consolidated Financial Statements", to certain entities in which equity investors do not have the characteristics of a controlling financial interest or do not have sufficient equity at risk for the entity to finance its activities without additional subordinated financial support from other parties. FIN 46 applies immediately to variable interest entities created after January 31, 2003, and to variable interest entities in which an enterprise obtains an interest after that date. It applies in the first fiscal year or interim periodperiods beginning after June 15, 2003,2005, and will require the Company to variable interest entities in which an enterprise holds a variable interest thatrecognize compensation cost based on the grant date fair value of the equity instruments it acquired before February 1, 2003.awards. The Company currently accounts for those instruments under the recognition and measurement principles of APB Opinion 25, including the disclosure-only provisions of the original SFAS 123. Accordingly, no compensation cost from issuing equity instruments has not identified and does not expect to identify any variable interest entitiesbeen recognized in the Company's financial statements. The Company estimates that must be consolidated. In December 2002, the Financial Accounting Standards Board issued SFAS 148 "Accounting for Stock-Based Compensation - Transition and Disclosure - an amendment of FASB Statement 123," which is effective for all fiscal years ending after December 15, 2002. SFAS 148 provides alternative methods of transition for a voluntary change to fair value based method of accounting for stock-based employee compensation under SFAS 123 from intrinsic value based method of accounting prescribed by Accounting Principles Board Opinion 25. SFAS 148 also changes the disclosure requirementrequired adoption of SFAS 123 requiring(R) in third quarter 2005 will have a more prominent disclosurenegative impact on its consolidated financial statements. Please see note 1, starting on page F-12 for an estimate of the pro-forma effect of the fair value based method of accounting for stock-based compensation. The adoption of SFAS 148 by the Company did notimpact this Statement would have any impacthad on the Company's consolidated financial statements and is not expected to have any impact on future operations.net income for the periods covered by this report. -24- ITEM 7A - QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK. Prior to January 1, 2002, theRISK The Company had manufacturing operations, including related assets, in Ireland denominated in Irish Pounds,the EURO, and sold products under agreements denominated in various Western European currencies. On January 1, 2002, UTMD converted its Irish operations and assets to the EURO currency, consistent with conversion of Ireland and many other Western European countries to the new common EURO currency. The EURO Irish Pound and other currencies have been and are subject to exchange rate fluctuations that are beyond the control of UTMD. The exchange rate for the EURO was .7335, .7958 and .9551 per U.S. Dollar as of December 31, 2004, 2003 and 2002, respectively. The exchange rate for the Irish Pound was .8869 per U.S. Dollar as of December 31, 2001. Please see Note 1, starting on page F-9.F-12. UTMD manages its foreign currency risk without separate hedging transactions by converting currencies as transactions occur. 25 ITEM 8 - FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA.DATA See index to financial statements and financial statement schedule at page F-1. ITEM 9 - CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE. On November 2, 2003, the Audit Committee of the Board of Directors of UTMD decided to engage Jones Simkins, P.C., Logan, Utah as independent accountant and auditor to report on UTMD's financial statements for the year ended December 31, 2003, and to complete quarterly reviews in 2004. In conjunction with the new engagement, UTMD discontinued the services of Tanner + Co., Salt Lake City, Utah as the Company's principal accountant to audit and report on the Company's financial statements. Tanner + Co. had served UTMD as external auditor for the last six years. Under SEC Regulation S-K, Reg ss.229.304, the reason for the auditor change was dismissal, not resignation for declining to stand for re-election. The report of Tanner + Co. on UTMD's financial statements consisting of consolidated balance sheets as of December 31, 2002 and 2001, and the related consolidated statements of income, stockholders' equity, and cash flows for each of the three years in the period ended December 31, 2002, did not contain an adverse opinion or disclaimer of opinion and was not qualified or modified as to audit scope or accounting principles. In addition to acting as UTMD's principal accountant, Tanner + Co. prepared UTMD's tax filings for the prior nine years and its quarterly reviews since such reviews have been required by SEC policies. Russell Brennan Keane, Athlone, Ireland has audited UTMD's Ireland subsidiary, Utah Medical Products Ltd., for the prior five years. In connection with the Company's two most recent fiscal year audits and any subsequent interim period preceding the disengagement of Tanner + Co., there were no disagreements with Tanner + Co. or reportable events on any matter of accounting principles or practices, financial statement disclosure, or auditing scope or procedure, which disagreement, if not resolved to the satisfaction of the former accountant, would have caused it to make reference to the subject matter of the disagreement in connection with its report. In connection with its audit of UTMD's 2002 financial statements, Tanner + Co. noted no matters involving the internal control structure and operations that they considered to be material weaknesses. The Audit Committee, comprised of UTMD's outside directors, believed a change in auditors would be beneficial to executing its oversight responsibilities by providing a fresh look at the Company's records and financial controls. The Audit Committee believes Jones Simkins has an experienced staff and partners well suited to serve the needs of UTMD. No consultations occurred between UTMD and Jones Simkins during the two most recent fiscal years and any subsequent interim period prior to Jones Simkins' appointment regarding either (i) the application of accounting principles to a specific completed or contemplated transaction, the type of audit opinion that might be rendered on UTMD's financial statements, or other information provided that was considered by the Company in reaching a decision as to an accounting, auditing, or financial reporting issue, or (ii) any matter that was the subject of disagreement or a reportable event requiring disclosure under Item 304(a)(1)(v) of Regulation S-K. 26 DISCLOSURE None. ITEM 9A - DISCLOSURE CONTROLS AND PROCEDURES.PROCEDURES Evaluation of Disclosure Controls and Procedures. UTMD maintains a system of internal controls and procedures designed to provide reasonable assurance as to the reliability of its consolidated condensed financial statements and other disclosures included in this report. UTMD's Board of Directors, operating through its audit committee, provides oversight to its financial reporting process. Within the 90-day period prior to the date of this report, UTMD evaluated the effectiveness of the design and operation of its disclosure controls and procedures pursuant to Rule 13a-14 of the Securities Exchange Act of 1934. Based on that evaluation, UTMD's Chief Executive Officer and Chief Financial Officer concluded that its disclosure controls and procedures are effective in alerting them in a timely manner to material information relating to UTMD required to be included in this annual report on Form 10-K. Management's Report on Internal Control Over Financial Reporting. Pursuant to Section 404 of the Sarbanes-Oxley Act of 2002, the Company has included, as part of this Form 10-K, a report of management's assessment of the effectiveness of its internal controls as of December 31, 2004. Jones Simkins, P.C., the independent registered public accounting firm of the Company, has audited management's assessment of, and the effectiveness of, the Company's internal control over financial reporting. Management's report, and the report of Jones Simkins, P.C. appear on pages F-2 and F-3 of this Form 10-K under the captions "Management's Report on Internal Control Over Financial Reporting" and "Report of Independent Registered Public Accounting Firm on Internal Control Over Financial Reporting" and are incorporated herein by reference. Changes in Internal Control Over Financial Reporting. There have been no significant changes in UTMD's internal controls or in other factors that could significantly affect internal controls subsequent to the date that it carried out its evaluation and there were no corrective actions regarding significant deficiencies or material weaknesses. [Remainder of Page Intentionally Left Blank] 27ITEM 9B- OTHER INFORMATION None. -25- PART III -------- ITEM 10 - DIRECTORS AND EXECUTIVE OFFICERS OF THE REGISTRANT. The information from the definitive proxy statement of the registrant under the caption, "PROPOSAL NO. 1. ELECTION OF DIRECTORS: General," "Directors and Nominees," "Executive Officers," and "Compliance with Exchange Act Requirements," is incorporated herein by reference, expressly excluding the material set forth under the subcaptions "Report of the Compensation and Option Committee" and "Stock Performance Chart." UTMD adopted a Code of Ethics for its executive officers, including the Chief Executive Officer, and outside directors in October 2003. The Code of Ethics, along with UTMD's Code of Conduct, which covers all exempt employees (including all officers and outside directors) and certain non-exempt employees, is posted on UTMD's web site at www.utahmed.com. UTMD intends to post on its website any waivers of or amendments to its Code of Ethics. ITEM 11 - EXECUTIVE COMPENSATION.COMPENSATION The information from the definitive proxy statement of the registrant under the caption, "PROPOSAL NO. 1. ELECTION OF DIRECTORS: Executive Compensation," "Compensation and Option Committee Interlocks and Insider Participation," "Employment Agreements, Termination of Employment, and Change in Control," and "Director's Compensation" is incorporated herein by reference, expressly excluding the material set forth under the subcaptions "Report of the Compensation and Option Committee" and "Stock Performance Chart." ITEM 12 - SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT.MANAGEMENT AND RELATED STOCKHOLDER MATTERS The information from the definitive proxy statement of the registrant under the caption, "PROPOSAL NO. 1. ELECTION OF DIRECTORS: Security Ownership of Management and Certain Persons" is incorporated herein by reference. ITEM 13 - CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS.TRANSACTIONS None. 28ITEM 14 - PRINCIPAL ACCOUNTANT FEES AND SERVICES The information from the definitive proxy statement for the 2005 annual meeting of stockholders under the caption "Independent Public Accountants" is incorporated herein by reference. -26- PART IV --------------- ITEM 1415 - EXHIBITS AND FINANCIAL STATEMENT SCHEDULES AND REPORTS ON FORM 8-K. (a) The following documents are filed as part of this report or incorporated herein by reference. 1. Financial Statements. (See Index to Consolidated Financial Statements at page F-1.) 2. Supplemental Schedule. Financial Statement Schedules are omitted because they are inapplicable or the required information is otherwise included in the accompanying Financial Statements and the notes thereto. 3. Exhibits.
SEC Exhibit # Reference # Title of Document Location - ---------- ----------- ------------------------------------------------------------------ ---------------- 1 3 Articles of Restatement of the Articles of Incorporation Incorporated by Reference (1) 2 3 Bylaws Incorporated by Reference (1) 3 4 Rights Agreement dated as of October 28, 1994, between Utah Incorporated by Medical Products, Inc., and Registrar and Transfer Company Reference (1) 4 4 Designation of Rights, Privileges, and Preferences of Series "A" Incorporated by Preferred Stock Reference (1) 5 10 Employment Agreement dated December 21, 1992 with Kevin L. This Filing Cornwell* 6 10 Amendment, effective May 15, 1998, to Employment Agreement dated This Filing December 21, 1992 with Kevin L. Cornwell* 7 10 Utah Medical Products, Inc., 2003 Employees' and Directors' Incorporated by Incentive Plan* Reference (2) 8 10 Utah Medical Products, Inc., 1994 Employee Incentive Stock Incorporated by Option Plan* Reference (1) 9 10 Loan Agreement, dated 3 July, 2002 between Utah Medical Incorporated by Products, Inc and U.S. Bank National Association Reference (3) 10 10 Revolving Promissory Note, dated July 3, 2002 by Utah Medical Incorporated by Products, Inc. to U.S. Bank National Association Reference (3) 11 10 First Amendment to Loan Agreement, dated 21 May 2003 between Incorporated by Utah Medical Products, Inc. and U.S. Bank National Association Reference (4) 12 21 Subsidiaries of Utah Medical Products, Inc. Incorporated by Reference (5) 13 23 Consent of Jones Simkins, P.C., Company's independent auditors This Filing for the year ending December 31, 2003 29 SEC Exhibit # Reference # Title of Document Location - --------- ----------- ----------------- -------- 14 23 Consent of Tanner + Co., Company's independent This Filing Auditors for the years ending December 31, 2002 and December 31, 2001 15 31 Certification of CEO pursuant to Rule 13a-14(a) as adopted This Filing pursuant to Section 302 of the Sarbanes-Oxley Act of 2002 16 31 Certification of Principal Financial Officer pursuant to Rule This Filing 13a-14(a) as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002 17 32 Certification of CEO pursuant to 18 U.S.C. ss.1350, as Adopted This Filing Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002 18 32 Certification of Principal Financial Officer pursuant to 18 This Filing U.S.C. ss.1350,SEC Exhibit # Reference # Title of Document Location - --------- ----------- -------------------------------------- --------------- 1 3 Articles of Restatement of the Articles This Filing of Incorporation 2 3 Articles of Correction to the Restated This Filing Articles of Incorporation 3 3 Bylaws Incorporated by Reference (1) 4 4 Rights Agreement dated as of July 30, Incorporated by 2004, between Utah Medical Products, Reference (2) Inc., and Registrar and Transfer Company 5 4 Designation of Rights, Privileges, and Incorporated by Preferences of Series "A" Preferred Stock Reference (1) 6 10 Employment Agreement dated December 21, Incorporated by 1992 with Kevin L. Cornwell* Reference (3) 7 10 Amendment, effective May 15, 1998, to Incorporated by Employment Agreement dated December 21, Reference (3) 1992 with Kevin L. Cornwell* 8 10 Utah Medical Products, Inc., 2003 Incorporated by Employees' and Directors' Incentive Plan* Reference (4) 9 10 Loan Agreement, dated 3 July, 2002 Incorporated by between Utah Medical Products, Inc and Reference (5) U.S. Bank National Association 10 10 Revolving Promissory Note, dated July 3, Incorporated by 2002 by Utah Medical Products, Inc. to Reference (5) U.S. Bank National Association 11 10 Second Amendment to Loan Agreement, Incorporated by dated 30 August 2004 between Utah Reference (6) Medical Products, Inc. and U.S. Bank National Association 12 10 Summary of Officer and Director This Filing Compensation 13 21 Subsidiaries of Utah Medical Products, Incorporated by Inc. Reference (7) 14 23 Consent of Jones Simkins, P.C., Company's This Filing independent auditors for the years ended December 31, 2004 and December 31, 2003 15 23 Consent of Tanner + Co., Company's This Filing independent auditors for the year ended December 31, 2002 -27- SEC Exhibit # Reference # Title of Document Location - --------- ----------- ---------------------------------------- ----------- 16 31 Certification of CEO pursuant to Rule This Filing 13a-14(a) as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002 17 31 Certification of Principal Financial This Filing Officer pursuant to Rule 13a-14(a) as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002 18 32 Certification of CEO pursuant to 18 U.S.C. This Filing 1350, as Adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
19 32 Certification of Principal Financial This Filing Officer pursuant to 18 U.S.C. 1350, as Adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002 * Management contract of compensatory plan or arrangement required to be filed pursuant to Item 14(c). (1) Incorporated by reference from the Company's registration statement on form S-8 filed with the Commission effective February 10, 19951995. (2) Incorporated by reference from the Company's report on form 8-K filed with the Commission on October 1, 2004. (3) Incorporated by reference from the Company's annual report on form 10-K filed with the Commission for the year ended December 31, 2003. (4) Incorporated by reference from the Company's annual report on form 10-K filed with the Commission for the year ended December 31, 2002. (3)(5) Incorporated by reference from the Company's quarterly report on form 10-Q filed with the Commission for the quarter ended June 30, 2002. (4)(6) Incorporated by reference from the Company's quarterly report on form 10-Q filed with the Commission for the quarter ended JuneSeptember 30, 2003. (5)2004. (7) Incorporated by reference from the Company's annual report on form 10-K filed with the Commission for the year ended December 31, 1999. (b) Reports on Form 8-K. On October 21, 2003, UTMD filed a report on Form 8-K, Item 12, Results of Operations and Financial Condition, reporting financial results for third quarter 2003. On November 7, 2003, UTMD filed a report on Form 8-K, Item 4, Changes in Registrant's Certifying Accountant, reporting the audit committee's decision to change UTMD's certifying accountant from Tanner + Co. to Jones Simkins, P.C. On December 5, 2003, UTMD filed a report on Form 8-K, Item 5, Other Items, reporting that the U.S. Court of Appeals affirmed a 2002 judgment by the Federal District Court awarding UTMD approximately $23 million in damages and accrued interest from Tyco International for patent infringement. 30-28- SIGNATURES Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned this 15th16th day of March, 2004.2005. UTAH MEDICAL PRODUCTS, INC. By: /s/ Kevin L. Cornwell -------------------------------------------------------------- Kevin L. Cornwell CEO Chief Executive Officer By: /s/ Greg A. LeClaire -------------------------------------------------------------- Greg A. LeClaire Chief Financial Officer Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following persons on behalf of the registrant and in the capacities indicated on this 15th16th day of March, 2004.2005. By: /s/ Stephen W. Bennett ----------------------------------------------------------------- Stephen W. Bennett, Director By: /s/ Kevin L. Cornwell ----------------------------------------------------------------- Kevin L. Cornwell, Director By: /s/ Ernst G. Hoyer ----------------------------------------------------------------- Ernst G. Hoyer, Director By: /s/ Barbara A. Payne ----------------------------------------------------------------- Barbara A. Payne, Director By: /s/ Paul O. Richins ----------------------------------------------------------------- Paul O. Richins, Director 31-29- UTAH MEDICAL PRODUCTS, INC. CONSOLIDATED FINANCIAL STATEMENTS December 31, 2004, 2003 2002 and 20012002 UTAH MEDICAL PRODUCTS, INC. --------------------------- Index to Consolidated Financial Statements ------------------------------------------ December 31, 2004, 2003 2002 and 20012002 -------------------------------- Page ---- Management's Report on Internal Control Over Financial Reporting F-2 Report of Jones Simkins, P.C. F-2on Management's Assessment on Internal Control Over Financial Reporting F-3 Report of Jones Simkins, P.C. on Financial Statements F-5 Report of Tanner + Co. F-3on Financial Statements F-6 Consolidated balance sheet F-4F-7 Consolidated statement of income and comprehensive income F-5F-8 Consolidated statement of cash flows F-6F-9 Consolidated statement of stockholders' equity F-7F-11 Notes to consolidated financial statements F-8F-12 F-1 MANAGEMENT'S REPORT ON INTERNAL CONTROL OVER FINANCIAL REPORTING Management of the Company is responsible for establishing and maintaining adequate internal control over financial reporting as defined in Rules 13a-15(f) and 15d-15(f) under the Securities Exchange Act of 1934. The Company's internal control over financial reporting is designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with accounting principles generally accepted in the United States of America ("GAAP"). The Company's internal control over financial reporting includes those policies and procedures that: - pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the Company; - provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with GAAP, and that receipts and expenditures of the Company are being made only in accordance with authorizations of management and directors of the Company; and - provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use or disposition of the Company's assets that could have a material effect on the financial statements. Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate. As required by Section 404 of the Sarbanes-Oxley Act of 2002, management assessed the effectiveness of the Company's internal control over financial reporting as of December 31, 2004. In making this assessment, management used the criteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission (COSO) in Internal Control-Integrated Framework. Based on our assessment and those criteria, management believes that the Company maintained effective internal control over financial reporting as of December 31, 2004. The Company's independent registered public accounting firm, Jones Simkins, P.C., has audited management's assessment of the Company's internal control over financial reporting as of December 31, 2004, and their report is shown on the next pages. By: /s/ Kevin L. Cornwell ------------------------- Kevin L. Cornwell Chief Executive Officer By: /s/ Greg A. LeClaire ------------------------- Greg A. LeClaire Chief Financial Officer F-2 REPORT OF INDEPENDENT AUDITORS'REGISTERED PUBLIC ACCOUNTING FIRM ------------------------------------------------------- We have audited management's assessment, included in the accompanying report titled Management's Report On Internal Control Over Financial Reporting, that Utah Medical Products, Inc. maintained effective internal control over financial reporting as of December 31, 2004, based on criteria established in Internal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO). Utah Medical Products, Inc.'s management is responsible for maintaining effective internal control over financial reporting and for its assessment of the effectiveness of internal control over financial reporting. Our responsibility is to express an opinion on management's assessment and an opinion on the effectiveness of the company's internal control over financial reporting based on our audit. We conducted our audit in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all material respects. Our audit included obtaining an understanding of internal control over financial reporting, evaluating management's assessment, testing and evaluating the design and operating effectiveness of internal control, and performing such other procedures as we considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion. A company's internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. A company's internal control over financial reporting includes those policies and procedures that (1) pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of the company are being made only in accordance with authorizations of management and directors of the company; and (3) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or disposition of the company's assets that could have a material effect on the financial statements. Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate. In our opinion, management's assessment that Utah Medical Products, Inc. maintained effective internal control over financial reporting as of December 31, 2004, is fairly stated, in all material respects, based on criteria established in Internal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO). F-3 Also in our opinion, Utah Medical Products, Inc. maintained, in all material respects, effective internal control over financial reporting as of December 31, 2004 based on criteria established in Internal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO). We have also audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the December 31, 2004 consolidated financial statements of Utah Medical Products, Inc. and our report dated January 17, 2005 expressed an unqualified opinion. /s/ Jones Simkins, P.C. - ----------------------- JONES SIMKINS, P.C. Logan, Utah January 17, 2005 F-4 REPORT OF INDEPENDENT REGISTERED -------------------------------- PUBLIC ACCOUNTING FIRM ---------------------- To the Board of Directors and Stockholders' of Utah Medical Products, Inc. We have audited the accompanying consolidated balance sheetsheets of Utah Medical Products, Inc. as of December 31, 2004 and 2003 and the related consolidated statements of income and comprehensive income, stockholders' equity, and cash flows for the years then ended. These consolidated financial statements are the responsibility of the Company's management. Our responsibility is to express an opinion on these consolidated financial statements based on our audits. We conducted our audits in accordance with generally accepted auditing standards as established by the Auditing Standards Board (United States) and in accordance with the auditing standards of the Public Company Accounting Oversight Board (United States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. An audit includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An audit also includes assessing the accounting principles used and significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe that our audits provide a reasonable basis for our opinion. In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial position of Utah Medical Products, Inc. as of December 31, 2004 and 2003 and the results of its operations and its cash flows for the years then ended in conformity with accounting principles generally accepted in the United States of America. We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the effectiveness of Utah Medical Products, Inc. internal control over financial reporting as of December 31, 2004, based on criteria established in Internal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO) and our report dated January 17, 2005 expressed an unqualified opinion. /s/ Jones Simkins, P.C. - ----------------------- JONES SIMKINS, P.C. Logan, Utah January 17, 2005 F-5 INDEPENDENT AUDITORS' REPORT To the Board of Directors and Stockholders of Utah Medical Products, Inc. We have audited the consolidated statements of income and other comprehensive income, stockholders' equity, and cash flows of Utah Medical Products, Inc. for the year ended December 31, 2003.2002. These consolidated financial statements are the responsibility of the Company's management. Our responsibility is to express an opinion on these consolidated financial statements based on our audit. We conducted our audit in accordance with auditing standards generally accepted in the United States of America. Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. An audit includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An audit also includes assessing the accounting principles used and significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe that our audit provides a reasonable basis for our opinion. In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial positionresults of operations and cash flows of Utah Medical Products, Inc. as of December 31, 2003 and the results of its operations and its cash flows for the year ended December 31, 2003 in conformity with accounting principles generally accepted in the United States of America. /s/ Jones Simkins, P.C. JONES SIMKINS, P.C. Logan, Utah January 20, 2004 F-2 INDEPENDENT AUDITORS' REPORT ---------------------------- To the Board of Directors and Stockholders of Utah Medical Products, Inc. We have audited the consolidated balance sheet of Utah Medical Products, Inc. as of December 31, 2002 and the related consolidated statements of income and other comprehensive income, stockholders' equity, and cash flows for the years ended December 31, 2002 and 2001. These consolidated financial statements are the responsibility of the Company's management. Our responsibility is to express an opinion on these consolidated financial statements based on our audits. We conducted our audits in accordance with auditing standards generally accepted in the United States of America. Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. An audit includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An audit also includes assessing the accounting principles used and significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe that our audits provide a reasonable basis for our opinion. In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial position of Utah Medical Products, Inc. as of December 31, 2002, and the results of their operations and their cash flows for the years ended December 31, 2002 and 2001 in conformity with accounting principles generally accepted in the United States of America. /s/ Tanner + CompanyCo. Salt Lake City, Utah January 21, 2003 F-3F-6 UTAH MEDICAL PRODUCTS, INC. --------------------------- CONSOLIDATED BALANCE SHEET -------------------------- December 31, 2004 and 2003 and 2002-------------------------- (In thousands) ASSETS 2004 2003 2002 ------ -------- -------- Current assets: Cash $ 1,818 $ 762 285 Investments, available-for-sale (note 3) 15,110 722 -- Accounts receivable, net (note 2) 3,730 3,326 3,093 Inventories (note 2) 2,859 3,268 3,478 Prepaid expenses and other current assets 263 219 502 Litigation receivable (note 13) -- 24,884 -- Deferred income taxes (note 7) 750 721 399 -------- -------- Total current assets 24,530 33,902 7,757 Property and equipment, net (note 4) 9,058 9,005 8,890 Other assets, net (note 2) 7,674 6,787 6,740 -------- -------- Total assets $ 41,262 $ 49,694 23,387 ======== ======== LIABILITIES AND STOCKHOLDERS' EQUITY ------------------------------------ Current liabilities: Accounts payable $ 698 $ 368 631 Accrued expenses (note 2) 3,638 12,129 1,688 -------- -------- Total current liabilities 4,336 12,497 2,319 Note payable (note 5) -- 4,956 Deferred income taxes (note 7) 769 665 390 -------- -------- Total liabilities 5,105 13,162 7,665 -------- -------- Commitments and contingencies (notes 6 and 10) -- -- Stockholders' equity: Preferred stock, $.01 par value; 5,000 shares authorized, no shares issued and outstanding -- -- Common stock, $.01 par value; 50,000 shares authorized, issued 4,105 shares in 2004 and 4,544 shares in 2003 and 4,443 shares in 200241 45 44 Accumulated other comprehensive income 226 (260) (1,115) Retained earnings 35,890 36,747 16,793 -------- -------- Total stockholders' equity 36,157 36,532 15,722 -------- -------- Total liabilities and stockholders' equity $ 41,262 $ 49,694 23,387 ======== ======== See accompanying notes to financial statements. F-4statements F-7
UTAH MEDICAL PRODUCTS, INC. --------------------------- CONSOLIDATED STATEMENT OF INCOME -------------------------------- AND COMPREHENSIVE INCOME ------------------------ Years Ended December 31, 2003, 2002 and 2001 -------------------------------------------- (In thousands, except per share amounts) ---------------------------------------- 2003 2002 2001 -------- -------- -------- Sales, net (note 9) $ 27,137 $ 27,361 $ 26,954 Cost of goods sold (notes 9 and 10) 11,245 11,598 11,561 -------- -------- -------- Gross margin 15,892 15,763 15,393 Operating expenses: Sales and marketing 2,364 2,472 2,773 Research and development 288 285 364 General and administrative 2,518 2,464 2,978 -------- -------- -------- Income from operations 10,722 10,542 9,278 Other income (expense): Dividend and interest income 5 6 9 Royalty income 450 450 450 Interest expense (47) (36) (370) Other, net 46 34 113 -------- -------- -------- Income before provision for income taxes and extraordinary item 11,176 10,996 9,480 Provision for income taxes (note 7) 3,841 3,831 3,546 -------- -------- -------- Income before extraordinary item 7,335 7,165 5,934 Extraordinary item - gain from litigation, net of income taxes of $9,250 (note 13) 13,426 -- -- -------- -------- -------- Net income $ 20,761 $ 7,165 $ 5,934 ======== ======== ======== Earnings per common share (basic) (notes 1 and 2): Before extraordinary item $ 1.62 $ 1.46 $ 1.18 Extraordinary item 2.97 -- -- -------- -------- -------- Total $ 4.59 $ 1.46 $ 1.18 ======== ======== ======== Earnings per common share (diluted) (notes 1 and 2): Before extraordinary item $ 1.50 $ 1.36 $ 1.14 Extraordinary item 2.75 -- -- -------- -------- -------- Total $ 4.25 $ 1.36 $ 1.14 ======== ======== ======== Other comprehensive income: Foreign currency translation net of taxes of $288, $244, and $(87)UTAH MEDICAL PRODUCTS, INC. --------------------------- CONSOLIDATED STATEMENT OF INCOME -------------------------------- AND COMPREHENSIVE INCOME ------------------------ Years ended December 31, 2004, 2003 and 2002 -------------------------------------------- (In thousands, except per share amounts) 2004 2003 2002 -------- -------- -------- Sales, net (note 9) $ 26,485 $ 27,137 $ 27,361 Cost of goods sold (notes 9 and 10) 11,419 11,245 11,598 -------- -------- -------- Gross margin 15,066 15,892 15,763 Operating expenses: Sales and marketing 2,253 2,364 2,472 Research and development 292 288 285 General and administrative 2,412 2,518 2,464 -------- -------- -------- Income from operations 10,109 10,722 10,542 Other income (expense): Dividend and interest income 238 5 6 Royalty income 450 450 450 Interest expense -- (47) (36) Other, net 110 46 34 -------- -------- -------- Income before provision for income taxes and extraordinary items 10,907 11,176 10,996 Provison for income taxes (note 7) 3,741 3,841 3,831 -------- -------- -------- Income before extraordinary items 7,166 7,335 7,165 Extraordinary items, net of income taxes of $2,156 in 2004 and $9,250 in 2003 (note 13) 3,054 13,426 -- -------- -------- -------- Net income $ 10,220 $ 20,761 $ 7,165 ======== ======== ======== Earnings per common share (basic) (notes 1 and 2): Before extraordinary items $ 1.63 $ 1.62 $ 1.46 Extraordinary items 0.69 2.97 -- -------- -------- -------- Total $ 2.32 $ 4.59 $ 1.46 ======== ======== ======== Earnings per common share (diluted) (notes 1 and 2): Before extraordinary items $ 1.53 $ 1.50 $ 1.36 Extraordinary items 0.65 2.75 -- -------- -------- -------- Total $ 2.19 $ 4.25 $ 1.36 ======== ======== ======== Other comprehensive income: Foreign currency translation net of taxes of $107, $288 and $244 $ 222 $ 548 $ 457 $ (170) Unrealized gain on investments net of taxes of $61, $12 $0, and $0 157 19 -- -- -------- -------- -------- Total comprehensive income $ 10,599 $ 21,328 $ 7,622 $ 5,764 ======== ======== ======== See accompanying notes to financial statements.
F-5F-8
UTAH MEDICAL PRODUCTS, INC. --------------------------- CONSOLIDATED STATEMENT OF CASH FLOW ----------------------------------- Years Ended December 31, 2004, 2003 2002 and 20012002 -------------------------------------------- (In thousands) --------------2004 2003 2002 2001 -------- -------- -------- Cash flows from operating activities: - ------------------------------------- Net income $ 10,220 $ 20,761 $ 7,165 $ 5,934-------- -------- -------- Adjustments to reconcile net income to net cash provided by operating activities: Depreciation and amortization 809 984 1,172 1,933 Gain on investments (52) (11) -- -- Provision for (recovery of) losses on accounts receivable 3 (93) 18 70 Loss on disposal of assets 5 4 -- 6 Deferred income taxes 75 (47) 108 (26) Tax benefit attributable to exercise of stock options 446 1,108 354 60 (Increase) decrease in: Accounts receivable (226) 36 577 164 Accrued interest and other receivables (191) 257 (316) 121 Inventories 437 174 (168) (239) Prepaid expenses and other current assets (43) (32) (31) (20) Litigation receivable 24,884 (24,884) -- -- Increase (decrease) in: Accounts payable 312 (291) 154 (208) Accrued expenses (9,220) 10,369 (377) 65 -------- -------- -------- Net cash provided by operating activities 27,459 8,335 8,656 7,860 -------- -------- -------- Cash flows from investing activities: - ------------------------------------- Capital expenditures for: Property and equipment (411) (272) (517) (524) Intangible assets (10) (122) -- -- PurchasePurchases of investments (22,103) (737) -- -- Proceeds from the sale of investments 8,202 98 -- Net cash paid in acquisition (1,012) -- -- -------- -------- -------- Net cash used in investing activities (15,334) (1,033) (517) (524) -------- -------- -------- Cash flows from financing activities: - ------------------------------------- Proceeds from issuance of common stock - options 1,111 882 1,113 316 Common stock purchased and retired (10,692) (2,240) (11,787) (193) Common stock purchased and retired - options (6) (555) (31) -- Proceeds from note payable -- -- 4,956 -- Repayments of note payable -- (4,956) (2,501) (7,499)Dividends paid (1,331) -- -- -------- -------- -------- Net cash used in financing activities (10,918) (6,869) (8,250) (7,376) -------- -------- -------- Effect of exchange rate changes on cash (151) 44 26 (4) -------- -------- -------- Net increase (decrease) in cash and cash equivalents 1,056 477 (85) (44) Cash at beginning of year 762 285 370 414 -------- -------- -------- Cash at end of year $ 1,818 $ 762 $ 285 $ 370 ======== ======== ======== Supplemental disclosures of cash flow information: - --------------------------------------------------- Cash paid during the year for: Income taxes $ 2,628 $ 3,568 $ 3,399 ======== ======== ======== Interest $ 47 $ 25 $ 370 ======== ======== ======== See accompanying notes to financial statements. F-6F-9
UTAH MEDICAL PRODUCTS, INC. --------------------------- CONSOLIDATED STATEMENT OF CASH FLOW ----------------------------------- Years Ended December 31, 2004, 2003 and 2002 -------------------------------------------- (In thousands) Continued SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION: 2004 2003 2002 -------- -------- -------- Cash paid during the year for: Income taxes $ 14,294 $ 2,628 $ 3,568 Interest $ -- $ 47 $ 25 During 2004, the Company purchased all of the oustanding stock of Abcorp Medical, Inc. The Company paid cash and recorded net assets from the acquisition as follows: Cash $ 11 Accounts receivable 127 Inventory 25 Prepaid insurance 19 Equipment, net 16 Accounts payable (96) Accrued expenses (25) Goodwill 946 -------- Total cash paid 1,023 Less cash received (11) -------- Net cash investment $ 1,012 See accompanying notes to financial statements. F-10
UTAH MEDICAL PRODUCTS, INC. --------------------------- CONSOLIDATED STATEMENT OF STOCKHOLDERS' EQUITY ---------------------------------------------- Years Ended December 31, 2004, 2003 2002 and 20012002 -------------------------------------------- (In thousands) -------------- Accumulated Common Stock Additional Other Total --------------------- Paid-In------------------- Paid-in Comprehensive Retained Stockholders' Shares Amount Capital Income Earnings Equity -------- -------- -------- -------- -------- -------- Balance at January 1, 2001 5,003 $ 50 $ -- $ (1,559) $ 13,856 $ 12,347 Shares issued upon exercise of employee stock options for cash 45 -- 316 -- -- 316 Tax benefit attributable to appreciation of stock options -- -- 60 -- -- 60 Common stock purchased and retired (19) -- (376) -- 183 (193) Foreign currency translation adjustment -- -- -- (257) -- (257) Net income -- -- -- -- 5,934 5,934 -------- -------- -------- -------- -------- -------- Balance at December 31, 2001 5,029 $ 50 $ -- $ (1,816) $ 19,973 $ 18,207 2002 Shares issued upon exercise of employee stock options for cash 137 1 1,112 -- -- 1,113 Shares received and retired upon exercise of stock options (2) -- (31) -- -- (31) Tax benefit attributable to appreciation of stock options -- -- 354 -- -- 354 Common stock purchased and retired (721) (7) (1,435) -- (10,345) (11,787) Foreign currency translation adjustment -- -- -- 701 -- 701 Net income -- -- -- -- 7,165 7,165 -------- -------- -------- -------- -------- -------- Balance at December 31, 2002 4,443 $ 44 $ -- $ (1,115) $ 16,793 $ 15,722 Shares issued upon exercise of employee stock options for cash 299 3 2,465 -- -- 2,468 Shares received and retired upon exercise of stock options (101) (1) (2,141) -- -- (2,142) Tax benefit attributable to appreciation of stock options -- -- 1,108 -- -- 1,108 Common stock purchased and retired (97) (1) (1,432) -- (807) (2,240) Foreign currency translation adjustment -- -- -- 836 -- 836 Unrealized holding gain from investments, available-for-sale, net of taxtaxes -- -- -- 19 -- 19 Net income -- -- -- -- 20,761 20,761 -------- -------- -------- -------- -------- -------- Balance at December 31, 2003 4,544 $ 45 $ -- $ (260) $ 36,747 $ 36,532 Shares issued upon exercise of employee stock options for cash 123 1 1,234 -- -- 1,235 Shares received and retired upon exercise of stock options (5) (0) (124) -- -- (124) Tax benefit attributable to appreciation of stock options -- -- 446 -- -- 446 Common stock purchased and retired (557) (5) (1,556) -- (9,130) (10,691) Foreign currency translation adjustment -- -- -- 329 -- 329 Unrealized holding gain from investments, available-for-sale, net of taxes -- -- -- 157 -- 157 Common stock dividends -- -- -- -- (1,947) (1,947) Net income -- -- -- -- 10,220 10,220 -------- -------- -------- -------- -------- -------- Balance at December 31, 2004 4,105 $ 41 $ -- $ 226 $ 35,890 $ 36,157 ======== ======== ======== ======== ======== ======== See accompanying notes to financial statements. F-7F-11
UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 1 - Summary of Significant Accounting Policies - --------------------------------------------------- Organization - ------------ Utah Medical Products, Inc. and its wholly owned subsidiaries, principally Utah Medical Products Ltd., which operates a manufacturing facility in Ireland, and Columbia Medical, Inc., (the Company) are in the business of producing specialized devices for the health carehealthcare industry. The Company's broad range of products includes those used in critical care areas and the labor and delivery departments of hospitals, as well as outpatient clinics and physician'sphysicians' offices. Products are sold in both domestic U.S. and international markets. Use of Estimates in the Preparation of Financial Statements - ----------------------------------------------------------- The preparation of financial statements in conformity with accounting principles generally accepted in the United States of America requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Although actual results could differ from those estimates, management believes it has considered and disclosed all relevant information in making its estimates that materially affect reported performance and current values. Principles of Consolidation - --------------------------- The consolidated financial statements include those of the Company and its subsidiaries. All intercompany accounts and transactions have been eliminated in consolidation. Cash and Cash Equivalents - ------------------------- For purposes of the consolidated statement of cash flows, the Company considers cash on deposit and short-term investments with original maturities of three months or less to be cash and cash equivalents. Investments - ----------- The Company classifies its investments as "available for sale." Securities classified as "available for sale" are carried in the financial statements at fair value. Realized gains and losses, determined using the specific identification method, are included in operations; unrealized holding gains and losses are reported as a separate component of accumulated other comprehensive income. Declines in fair value below cost that are other than temporary are included in operations. F-8F-12 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 1 - Summary of Significant Accounting Policies (continued) - --------------------------------------------------------------- Concentration of Credit Risk - ---------------------------- The primary concentration of credit risk consists of trade receivables. In the normal course of business, the Company provides credit terms to its customers. Accordingly, the Company performs ongoing credit evaluations of its customers and maintains allowances for possible losses which, when realized, have been within the range of management's expectations as reflected by its reserves. The Company's customer base consists primarily of hospitals, medical product distributors, physician practices and others directly related to healthcare providers. Although the Company is affected by the well-being of the global healthcare industry, management does not believe significant trade receivable credit risk exists at December 31, 2003.2004. The Company maintains its cash in bank deposit accounts, which at times, may exceed federally insured limits in addition to Fidelity Investments'Investments accounts. The Company has not experienced any losses in such accounts and believes it is not exposed to a significant credit risk on cash and cash equivalent balances. Inventories - ----------- Finished products, work-in-process, and raw materials and supplies inventories are stated at the lower of cost (computed on a first-in, first-out method) or market (see Note 2). Property and Equipment - ---------------------- Property and equipment are stated at cost. Depreciation and amortization are computed using the straight-line and units-of-production methods over estimated useful lives as follows: Building and improvements 30-40 years Furniture, equipment and tooling 3-10 years Long-Lived Assets - ----------------- The Company evaluates its long-lived assets in accordance with SFASStatement of Financial Accounting Standards (SFAS) No. 144, "Accounting for the Impairment of Long-Lived Assets".Assets." Long-lived assets held and used by the Company are reviewed for impairment whenever events or changes in circumstances indicate that their net book value may not be recoverable. When such factors and circumstances exist, the Company compares the projected undiscounted future cash flows associated with the related asset or group of assets over their estimated useful lives against their respective carrying amounts. Impairment, if any, is based on the excess of the carrying amount over the fair value of those assets and is recorded in the period in which the determination was made. F-9F-13 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 1 - Summary of Significant Accounting Policies (continued) - ------------------------------------------------------------------------------------------------------------------ Intangible Assets - ----------------- Costs associated with the acquisition of patents, trademarks, license rights and non-compete agreements are capitalized and are being amortized using the straight-line method over periods ranging from 5 to 17 years. On January 1, 2002,The Company evaluates the Company adoptedcarrying value of its goodwill in accordance with SFAS No. 142, "Goodwill and Other Intangible Assets". SFAS No. 142 changes the accounting for goodwill and intangible assets with indefinite lives from an amortization method to an impairment approach. Other intangible assets will continue to be amortized over their estimated useful lives. Amortization of goodwill which relates to the Company's 1997 and 1998 acquisitions ceased on January 1, 2002. Goodwill amortization expense in 2001was (in thousands) $569. The Company has completed its annual impairment test of goodwill required by SFAS No. 142 andAssets." At December 31, 2004 no impairment was indicated. Loans to Related Parties - ------------------------ Except as further disclosed in these notes, the Company has not made loans to related entities including employees, directors, shareholders, suppliers or customers, nor does it guarantee the debt of related entities. Revenue Recognition - ------------------- Revenue from product sales is generally recognized at the time the product is shipped and invoiced and collectibility is reasonably assured. The Company also provides for the estimated cost that may be incurred for product warranties and unforeseen uncollectible accounts. The Company believes that revenue should be recognized at the time of shipment as title generally passes to the customer at the time of shipment. This policy meets the criteria of Staff Accounting Bulletin 101 in that there is persuasive evidence of an existing contract or arrangement, delivery has occurred, the price is fixed and determinable and the collectibility is reasonably assured. Income Taxes - ------------ The Company accounts for income taxes under SFAS No. 109, "Accounting for Income Taxes," whereby deferred taxes are computed under the asset and liability method. Legal Costs - ----------- The Company has been and continues to be involved in lawsuits which are an expected and at times unexpected consequence of its operations and in the ordinary course of business. The Company is currently involved in litigation with the FDA which it does not consider an expected consequence of its operations, or in the ordinary course of its business. The Company maintains a reserve for legal costs consistent with its previous experience and anticipated costs. The reserve for legal costs at December 31, 20032004 and 20022003 was (in thousands) $1,050$1,260 and $125,$1,050, respectively (see Note 2). F-10F-14 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 1 - Summary of Significant Accounting Policies (continued) - ------------------------------------------------------------------------------------------------------------------- Earnings per Share - ------------------ The computation of basic earnings per common share is based on the weighted average number of shares outstanding during each year. The computation of earnings per common share assuming dilution is based on the weighted average number of shares outstanding during the year plus the weighted average common stock equivalents which would arise from the exercise of stock options outstanding using the treasury stock method and the average market price per share during the year. The shares (in thousands) used in the computation of the Company's basic and diluted earnings per share are reconciled as follows: 2004 2003 2002 2001 ------ ------ ------ Weighted average number of shares outstanding - basic 4,399 4,526 4,913 5,019 Dilutive effect of stock options 276 359 350 191 ------ ------ ------ Weighted average number of shares outstanding, assuming dilution 4,675 4,885 5,263 5,210 ===== ===== =========== ====== ====== Stock-Based Compensation - ------------------------ At December 31, 2003,2004, the Company has stock-based employee compensation plans, which are described more fully in Note 8. The Company accounts for those plans under the recognition and measurement principles of APB Opinion 25, "Accounting for Stock Issued to Employees",Employees," and related Interpretations, and has adopted the disclosure-only provisions of SFAS 123, "Accounting for Stock-Based Compensation." Accordingly, no compensation cost has been recognized in the financial statements, as all options granted under those plans had an exercise price equal to or greater than the market value of the underlying common stock on the date of grant. Starting July 1, 2005, in accordance with SFAS 123 (revised 2004), the Company will be required to begin recognizing compensation cost related to its stock option plans. Please see note 14, below. Had compensation cost for the Company's stock option plans been determined based on the fair value at the grant date for awards starting in 1995 consistent with the provisions of SFAS 123, the Company's net earnings and earnings per share would have been reduced to the pro forma amounts indicated below (in thousands, except per share amounts): F-11F-15 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 1 - Summary of Significant Accounting Policies (continued) - ------------------------------------------------------------------------------------------------------------------- Stock-Based Compensation (continued) - -------------------------
Years ended December 31, ----------------------------------- 2003 2002 2001 ---------- ---------- --------- Net income as reported $ 20,761 $ 7,165 $ 5,934 Deduct: Total stock-based employee compensation expense determined under fair value based method for all awards, net of related tax effects (178) (175) (248) ---------- ---------- --------- Net income pro forma $ 20,583 $ 6,990 $ 5,686 ========== ==========Years ended December 31, -------------------------------------- 2004 2003 2002 ------------ ----------- --------- Net income as reported $ 10,220 $ 20,761 $ 7,165 Deduct: Total stock-based employee compensation expense determined under fair value based method for all awards, net of related tax effects (388) (178) (175) ------------ ----------- --------- Net income pro forma $ 9,832 $ 20,583 $ 6,990 ============ =========== ========= Earnings per share: Basic - as reported $ 2.32 $ 4.59 $ 1.46 ============ =========== ========= Basic - pro forma $ 2.24 $ 4.55 $ 1.42 ============ =========== ========= Diluted - as reported $ 2.19 $ 4.25 $ 1.36 ============ =========== ========= Diluted - pro forma $ 2.10 $ 4.21 $ 1.33 ============ =========== ========= Earnings per shared: Basic - as reported $ 4.59 $ 1.46 $ 1.18 ========== ========== ========= Basic - pro forma $ 4.55 $ 1.42 $ 1.13 ========== ========== ========= Diluted - as reported $ 4.25 $ 1.36 $ 1.14 ========== ========== ========= Diluted - pro forma $ 4.21 $ 1.33 $ 1.09 ========== ========== =========
Translation of Foreign Currencies - --------------------------------- Assets and liabilities of the Company's foreign subsidiary are translated into U.S. dollars at the applicable exchange rates at year-end. Net gains or losses resulting from the translation of the Company's assets and liabilities are reflected as a separate component of stockholders' equity. A negative translation impact on stockholders' equity reflects a current relative U.S. Dollar value higher than at the point in time that assets were actually acquired in a foreign currency. A positive translation impact would result from a U.S. Dollardollar weaker in value than at the point in time foreign assets were acquired. Income and expense items are translated at the weighted average rate of exchange (based on when transactions actually occurred) during the year. F-12F-16 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 2 - Detail of Certain Balance Sheet Accounts - ------------------------------------------------- December 31, ----------------------------------------------- 2004 2003 2002 -------- -------- Account receivable (in thousands): Receivables $ 3,3733,636 $ 3,2523,373 Accrued interest and other 171 27 8 Less allowance for doubtful accounts (77) (74) (167) -------- -------- $ 3,3263,730 $ 3,0933,326 ======== ======== Inventories (in thousands): Finished products $ 932 $ 1,495 $ 1,236 Work-in-process 640 631 907 Raw materials 1,287 1,142 1,335 -------- -------- $ 3,2682,859 $ 3,4783,268 ======== ======== Other assets (in thousands): Goodwill $ 8,5339,479 $ 8,533 Patents 2,025 2,015 1,893 License rights 293 293 Trademarks 224 224 Non-compete agreements $ 175 175 -------- -------- 12,196 11,240 11,118 Accumulated amortization (4,522) (4,453) (4,378) -------- -------- $ 6,7877,674 $ 6,7406,787 ======== ======== Accrued expenses (in thousands): Income taxes payable $ 9,270384 $ --9,270 Payroll and payroll taxes 963 1,479 1,019 Reserve for litigation costs 1,260 1,050 125Dividends payable 616 -- Other 415 330 544 -------- -------- $ 12,1293,638 $ 1,68812,129 ======== ======== The following table reflects a comparison of net income and net income per share for each of the three years ended December 31, adjusted to give effect to the adoption of SFAS 142 (in thousands, except per share amounts): F-13 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 2 - Detail of Certain Balance Sheet Accounts (continued) - ------------------------------------------------- 2003 2002 2001 ---- ---- ---- Reported net income $ 20,761 $ 7,165 $ 5,934 Add-back goodwill amortization, net of taxes - - 484 -------- --------- --------- 484 Adjusted net income $ 20,761 $ 7,165 $ 6,418 ======== ========= ========= Reported earnings per share - basic $ 4.59 $ 1.46 $ 1.18 Add-back goodwill amortization - - .10 -------- --------- --------- Adjusted earnings per share - basic $ 4.59 $ 1.46 $ 1.28 ======== ========= ========= Reported earnings per share - diluted $ 4.25 $ 1.36 $ 1.14 Add-back goodwill amortization - - .09 -------- --------- --------- Adjusted net income per share - diluted $ 4.25 $ 1.36 $ 1.23 ======== ========= ========= During the years ended December 31, 20032004 and 2002,2003, the carrying amount of goodwill remained unchanged atincreased (in thousands) $8,533$946 due to the Abcorp acquisition, which is described in detail in the consolidated statement of cash flow under "Supplemental Disclosure of Cash Flow Information". F-17 Note 3 - Investments - -------------------- The Company's investments, classified as available-for-sale consist of the following (in thousands): December 31, ----------------------------- 2004 2003 2002 ---- ----------- ------- Investments, aTat cost $14,822 $ 691 $ - Unrealized holding gain 288 31 - --------------- ------- Investments, at fair value $15,110 $ 722 $ - =============== ======= Changes in the unrealized holding gain on investment securities available-for-sale and reported as a separate component of accumulated other comprehensive income are as follows (in thousands): December 31, ----------------- 2004 2003 2002 ---- ----------- ------- Balance, beginning of year $ -19 $ - Unrealized holding gain 257 31 - Deferred income taxes on unrealized holding gain (100) (12) - ---------------- ------- Balance, end of year $ 176 $ 19 $ - ========= ======= F-14 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 --------------------------------======= Note 4 - Property and Equipment - ------------------------------- Property and equipment consists of the following (in thousands): 2004 2003 2002 --------------- -------- Land $ 1,0521,089 $ 9801,052 Buildings and improvements 9,283 8,738 7,816 Furniture, equipment and tooling 13,763 13,966 14,113 Construction-in-progress 41 111 190 -------- -------- 24,176 23,867 23,099 Accumulated depreciation and amortization (15,118) (14,862) (14,209) --------------- -------- $ 9,0059,058 $ 8,8909,005 ======== ======== F-18 Note 4 - Property and Equipment (continued) - ------------------------------------------- Included in the Company's consolidated balance sheet are the assets of its manufacturing facilities in Utah, Oregon and Ireland. Property and equipment, by location, are as follows (in thousands):
December 31, 2003 ----------------- Utah Oregon Ireland Total --------- -------- ------- -------- Land $ 621 $ - $ 431 $ 1,052 Building and improvements 4,082 32 4,624 8,738 Furniture, equipment, and tooling 11,901 1,245 820 13,966 Construction-in-progress 111 - - 111 --------- -------- ------- -------- Total 16,715 1,277 5,875 23,867 Accumulated depreciation and amortization (12,221) (1,267) (1,374) (14,862) --------- -------- ------- -------- Property and equipment, net $ 4,494 $ 10 $ 4,501 $ 9,005 =========December 31, 2004 ----------------- Utah Oregon Ireland Total -------- -------- -------- -------- Land $ 621 $ -- $ 468 $ 1,089 Building and improvements 4,234 32 5,017 9,283 Furniture, equipment and tooling 11,627 1,245 891 13,763 Construction-in-progress 41 -- -- 41 -------- -------- -------- -------- Total 16,523 1,277 6,376 24,176 Accumulated depreciation and amortization (12,224) (1,271) (1,623) (15,118) -------- -------- -------- -------- Property and equipment, net $ 4,299 $ 6 $ 4,753 $ 9,058 ======== ======== ======== ======== ======= ========
F-15 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003 2002----------------- Utah Oregon Ireland Total -------- -------- -------- -------- Land $ 621 $ -- $ 431 $ 1,052 Building and 2001 -------------------------------- Note 4 -improvements 4,082 32 4,624 8,738 Furniture, equipment and tooling 11,901 1,245 820 13,966 Construction-in-progress 111 -- -- 111 -------- -------- -------- -------- Total 16,715 1,277 5,875 23,867 Accumulated depreciation and amortization (12,221) (1,267) (1,374) (14,862) -------- -------- -------- -------- Property and Equipment (continued) - --------------------------------
December 31, 2002 ----------------- Utah Oregon Ireland Total --------- ---------- ----------- ---------- Land $ 621 $ - $ 359 $ 980 Building and improvements 3,931 32 3,853 7,816 Furniture, equipment, and tooling 12,111 1,244 758 14,113 Construction-in-progress 190 - - 190 --------- ---------- ----------- ---------- Total 16,853 1,276 4,970 23,099 Accumulated depreciation and amortization (11,862) (1,256) (1,091) (14,209) --------- ---------- ----------- ---------- Property and equipment, net $ 4,991 $ 20 $ 3,879 $ 8,890 ========= ========== =========== ==========
equipment, net $ 4,494 $ 10 $ 4,501 $ 9,005 ======== ======== ======== ======== F-19 Note 5 - Note Payable - --------------------- The Company has an unsecured bank line-of-credit agreement which allows the Company to borrow up to a fixed maximum amount (in thousands) of $15,000$5,000 at an interest rate equal to either the bank's LIBOR rate plus 1.25%, the bank's prime rate less 1.00%, or a daily rate based on LIBOR plus 1.35%. The line-of-credit-balance matures on May 31, 20052006 and hashad an outstanding balance of (in thousands) $0 and $4,956 at both December 31, 20032004 and 2002, respectively.2003. The principal financial loan covenants are a restriction on the total amount available for borrowing to 1.25 times the last twelve months' EBITDA, which as of December 31, 20032004 and 20022003 was equal to (in thousands) $43,506$21,158 and $15,255,$43,506, respectively, and a requirement to maintain a net worth in excess of $10 million, which at the end of 20032004 and 20022003 was (in thousands) $36,157 and $36,532, and $15,722, respectively. F-16 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 6 - Commitments and Contingencies - -------------------------------------- Operating Leases - ---------------- The Company has a lease agreement for land adjoining the Company'sits Utah facility for a term of forty years commencing on September 1, 1991. On September 1, 2001 and subsequent to each fifth lease year, the basic rental was and will be adjusted for published changes in a price index. The Company also leases its CMI building in Oregon under a short-termtwo-year noncancelable operating lease. Rent expense charged to operations under these operating lease agreements was approximately (in thousands) $107, $105 $104, and $101$104 for the years ended December 31, 2004, 2003 2002 and 2001,2002, respectively. Future minimum lease payments under its lease obligations as of December 31, 20032004 were as follows (in thousands): Years ending December 31: Amount ------------------------- ------ 20042005 $ 66 2005 37107 2006 3766 2007 37 2008 37 2009 37 Thereafter 851 --------808 --------- Total future minimum lease payments $ 1,065 ========1,092 ========= F-20 Note 6 - Commitments and Contingencies (continued) - -------------------------------------------------- Product Liability - ----------------- The Company is self-insured for product liability risk. "Product liability" is an insurance industry term for the cost of legal defense and possible eventual damages awarded as a result of use of a company's product during a procedure that results in an injury of a patient. The Company maintains a reserve for product liability litigation and damages consistent with its previous long-term experience. Actual product liability litigation costs and damages during the last three reporting years have been immaterial which is consistent with the Company's overall history. The Company absorbs the costs of clinical training, trouble-shooting and product warranties in its on-going operating expenses. Litigation - ---------- The Company has been involved in lawsuits which are an expected consequence of its operations and in the ordinary course of business. TheThere are no such lawsuits currently pending. With respect to the current litigation with the FDA, the Company believeshas always strongly maintained that pending litigation will not haveit is in substantial compliance with all government regulations. If the U.S. Court disagrees with the Company, there may be a materialmaterially adverse effect on itsthe Company's financial condition or results of operations. F-17 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002Alternatively, if the U.S. Court agrees with it, the Company may have the opportunity to seek restitution of litigation costs and 2001 -------------------------------- Note 6 - Commitments and Contingencies (continued) - --------------------------------------damages. The final pretrial conference is scheduled for June 20, 2005. Irish Development Agency - ------------------------ In order to satisfy requirements of the Irish Development Agency in assisting the start-up of its Ireland subsidiary, the Company agreed to invest certain amounts and maintain a certain capital structure in its Ireland subsidiary. The effect of these financial relationships and commitments are reflected in the consolidated financial statements and do not represent any significant credit risk that would affect future liquidity. F-21 Note 7 - Income Taxes - --------------------- Deferred tax assets (liabilities) consist of the following temporary differences (in thousands):
December 31, ------------ 2003 2002 ---- ---- Current Long-term Current Long-term -------- ---------- ------- --------- Inventory write-downs and differences due to UNICAP $ 169 $ - $ 178 $ - Allowance for doubtful accounts 29 - 57 - Accrued liabilities and reserves 523 12 164 - Other - 22 - - Depreciation and amortization - 164 - 162 Earnings from subsidiary - (863) - (552) -------- ---------- ------- --------- Deferred income taxes, net $ 721 $ (665) $ 399 $ (390) ======== ========= ======= ======== The components of income tax expense are as follows (in thousands): Years ended December 31, ------------------------ 2003 2002 2001 ---- ---- ---- Current $ 3,888 $ 3,715 $ 3,520 Deferred (47) 116 26 ------- ------ ------December 31, ------------ 2004 2003 ---- ---- Current Long-term Current Long-term ------- --------- ------- --------- Inventory write-downs and differences due to UNICAP $ 73 $ -- $ 169 $ -- Allowance for doubtful accounts 30 -- 29 -- Accrued liabilities and reserves 641 23 523 12 Other 6 (42) -- 22 Depreciation and amortization -- 161 -- 164 Earnings from subsidiary -- (911) -- (863) ----- ----- ----- ----- Deferred income taxes, net $ 750 $(769) $ 721 $(665) ===== ===== ===== ===== The components of income tax expense are as follows (in thousands): Years ended December 31, ------------------------ 2004 2003 2002 ---- ---- ---- Current $ 3,666 $ 3,888 $ 3,715 Deferred 75 (47) 116 ----- ----- ----- Total $ 3,741 $ 3,841 $ 3,831 $ 3,546 ===== ===== ===== Income tax expense differed from amounts computed by applying the statutory federal rate to pretax income as follows (in thousands):
F-18 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 7 - Income Taxes (continued) - --------------------- Years ended December 31, ------------------------ 2004 2003 2002 2001 --------- ---------- -------------- ---- ---- Federal income tax expense at the statutory rate $ 3,709 $ 3,716 $ 3,738 $ 3,062 State income taxes 545 559 482 474 ETI, foreign sales corporation and tax credits (164) (68) (182) (60) Other (349) (366) (207) 70 --------- ---------- --------------- ----- ----- Total $ 3,741 $ 3,841 $ 3,831 $ 3,546 ========= ========== =============== ===== ===== F-22 Note 8 - Options - ---------------- The Company has stock option plans which authorize the grant of stock options to eligible employees, directors and other individuals to purchase up to an aggregate of 2,200,0001,014,226 shares of common stock, of which 759,101755,526 are outstanding as of December 31, 2003.2004. All options granted under the plans are granted at current market value at date of grant, and may be exercised between six months and ten years following the date of grant. The plans are intended to advance the interest of the Company by attracting and ensuring retention of competent directors, employees and executive personnel, and to provide incentives to those individuals to devote their utmost efforts to the advancement of the Company. Changes in stock options were as follows: Price Range 2004 Shares Per Share ------ --------- Granted 164,100 $ 18.00 - $ 25.59 Expired or canceled 44,767 6.75 - 25.59 Exercised 122,908 6.50 - 17.71 Total outstanding at December 31 755,526 6.50 - 25.59 Total exercisable at December 31 554,727 6.50 - 24.02 Price Range 2003 Shares Per Share ------ --------- Granted 82,200 $ 17.71 - $ 24.02 Expired or canceled 12,562 6.75 - 17.71 Exercised 298,852 6.50 - 15.01 Total outstanding at December 31 759,101 6.50 - 24.02 Total exercisable at December 31 625,859 6.50 - 14.60 Price Range 2002 Shares Per Share ------ --------- Granted 74,100 $ 14.60 - $ 15.01 Expired or canceled 31,574 6.50 - 15.01 Exercised 137,089 6.50 - 14.25 Total outstanding at December 31 988,315 6.50 - 15.01 Total exercisable at December 31 870,414 6.50 - 14.25 Price Range 2001 Shares Per Share ------ --------- Granted 81,400 $ 9.13 - $ 12.00 Expired or canceled 28,855 6.50 - 14.25 Exercised 44,500 6.50 - 11.50 Total outstanding at December 31 1,082,878 6.50 - 14.25 Total exercisable at December 31 912,185 6.50 - 14.25 F-19 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 8 - Options (continued) - ---------------- For the years ended December 31, 2004, 2003 2002 and 2001,2002, the Company reduced current income taxes payable and increased additional paid-in capital by (in thousands) $446, $1,109 $354 and $60,$354, respectively, for the income tax benefit attributable to sale by optionees of common stock received upon the exercise of stock options. F-23 Note 8 - Options (continued) - ---------------------------- Stock-Based Compensation - ------------------------ The Company has adopted the disclosure-only provisions of Statement of Financial Accounting Standards (SFAS)SFAS No. 123, "Accounting for Stock-Based Compensation," as described in Note 1. The fair value of each option grant is estimated on the date of grant using the Black-Scholes option pricing model with the following weighted average assumptions: Years ended December 31, ------------------------ 2004 2003 2002 2001 ---- ---- ---- Expected dividend yield -0.7% - - Expected stock price volatility 39.0% 40.5% 41.7% 44.6% Risk-free interest rate (weighted average) 3.7% 3.5% 4.3% 4.9% Expected life of options 6.2 years 5.9 years 5.2 years 5.0 years The per-share weighted average fair value of options granted during 2004, 2003 and 2002 is $10.07, $8.89 and 2001 is $8.89, $6.52, and $4.27, respectively. F-20 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 8 - Options (continued) - ---------------- Stock-Based Compensation (continued) - ------------------------ The following table summarizes information about stock options outstanding at December 31, 2003:2004: Options Outstanding Options Exercisable --------------------------------- -------------------------------------------------------------- -------------------- Weighted Average Remaining Weighted Weighted Range of Contractual Average Average Exercise Number Life Exercise Number Exercise Prices Outstanding (Years) Price Exercisable Price ------- ----------------- ----------- ------- ----- ----------- ----- $ 6.50 - 7.75 307,634 4.707.25 276,052 3.71 $ 6.84 304,8706.83 276,052 $ 6.846.83 9.125 - 24.02 451,467 4.71 13.68 320,989 12.20 ---------------15.01 280,068 2.97 12.81 260,510 12.72 17.71 - 25.59 199,406 9.03 22.72 18,165 20.32 ---------------- ------- ---- ----- ------------- ----- $ 6.50 - 24.02 759,101 4.7025.59 755,526 4.84 $ 10.91 625,85913.24 554,727 $ 9.5910.04 =============== ======= ==== ===== ======= ========= F-24 Note 9 - Geographic Sales Information - ------------------------------------- The Company had sales in the following geographic areas (in thousands): United States Europe Other ------------- ------ ----- 2004 $ 20,452 $ 3,639 $ 2,394 2003 $ 21,266 $ 3,376 $ 2,495 2002 $ 21,626 $ 3,337 $ 2,398 2001 $ 21,752 $ 3,012 $ 2,190 Note 10 - Product Sale and Purchase Commitments - ----------------------------------------------- The Company has license agreements for the rights to develop and market certain products or technologies owned by unrelated parties. The confidential terms of such agreements are unique and varied, depending on many factors relating to the value and stage of development of the technology licensed. Royalties on future product sales are a normal component of such agreements and are included in the Company's cost of goods sold on an ongoing basis. The Company has in the past received and continues to receive royalties as a result of license agreements with unrelated companies that allow exclusive or nonexclusive rights to the Company's technology. F-21 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 11 - Employee Benefit Plan - ------------------------------- The Company has a contributory 401(k) savings plan for employees, who are at least 21 years of age, work 30 hours or more each week, and have a minimum of one year of service with the Company. The Company's contribution is determined annually by the board of directors. Company contributions were approximately (in thousands) $92, $95 $94 and $85$94 for the years ended December 31, 2004, 2003 2002 and 2001,2002, respectively. Note 12 - Fair Value Financial Instruments - ------------------------------------------ None of the Company's financial instruments, which are current assets and liabilities that could be readily traded, are held for trading purposes.purposes, except investments. Detail on investments is provided in note 3, above. The Company estimates that the fair value of all financial instruments at December 31, 2003,2004, does not differ materially from the aggregate carrying value of its financial instruments recorded in the accompanying consolidated balance sheet. F-25 Note 13 - Extraordinary ItemItems - --------------------------------------------------------- In December 2003,fourth quarter 2004, the Company recognized extraordinary non-operating incomeexpense of (in thousands) $24,884 including$500 resulting from increasing the Company's reserve for litigation expenses related to the litigation process with the U.S. Food & Drug Administration. Taxes on the expense were (in thousands) $204, resulting in a decrease to 2004 net income of $296. In January 2004, the Company received a payment of (in thousands) $30,944 in damages and interest resulting from thea 2002 District Federal Court judgment relating to the Company's patent infringement litigation against Tyco/Kendall-LTP, which was upheld by appellate court decision.KendalloLTP. The Company recognized extraordinary non-operating income from that payment of (in thousands) $6,060 in first quarter 2004 and (in thousands) $24,884 in fourth quarter 2003. After subtraction of additional expenses of (in thousands) $350 and income taxes of (in thousands) $2,361, the extraordinary income adds (in thousands) $3,349 to 2004 net income. Likewise, after subtraction of additional expenses of (in thousands) $2,208 and income taxes of (in thousands) $9,250, the extraordinary income adds (in thousands) $13,426 to 2003 net income. The actual payment from Tyco, which was received on January 20, 2004, included an additional approximately (in thousands) $6,000 in augmented damages and interest which will be recognized as an extraordinary gain in the first quarter 2004. Note 14 - Recent Accounting Pronouncements - ------------------------------------------ In May 2003,December 2004, the FASB issued SFAS 150,123 (revised 2004), "Accounting for Certain Financial Instruments with Characteristics of both Liabilities and Equity.Stock Based Compensation." This new statement changessupersedes APB Opinion No. 25, "Accounting for Stock Issued to Employees." This revised statement establishes standards for the accounting of transactions in which an entity exchanges its equity instruments for certain financial instruments that, under previous guidance, issuers could account for as equity or classifications between liabilitiesgoods and equity in a section that has been known as "mezzanine capital." It requires that those certain instruments be classified as liabilities in balance sheets. Mostservices, including the grant of the guidance in SFAS 150stock options to employees and directors. The statement is effective for all financial instruments entered into or modified after May 31, 2003. The adoption of SFAS 150 did not have any impact on the Company's consolidated financial statements. F-22 UTAH MEDICAL PRODUCTS, INC. --------------------------- NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ------------------------------------------ December 31, 2003, 2002 and 2001 -------------------------------- Note 14 - Recent Accounting Pronouncements (continued) - ------------------------------------------ In April 2003, the FASB issued SFAS 149, "Amendment of Statement 133 on Derivative Instruments and Hedging Activities." SFAS 149 amends and clarifies financial accounting and reporting for derivative instruments, including certain derivative instruments embedded in other contracts (collectively referred to as derivatives) and for hedging activities under SFAS 133, "Accounting for Derivative Instruments and Hedging Activities". This Statement is effective for contracts entered into or modified after June 30, 2003, with certain exceptions, and for hedging relationships designated after June 30, 2003, with certain exceptions. The adoption of SFAS 149 did not have any effect on the Company's consolidated financial statements. In January 2003, the FASB issued Interpretation 46, "Consolidation of Variable Interest Entities" (FIN 46), which addresses consolidation by business enterprises of variable interest entities. FIN 46 clarifies the application of Accounting Research Bulletin No. 51, "Consolidated Financial Statements", to certain entities in which equity investors do not have the characteristics of a controlling financial interest or do not have sufficient equity at risk for the entity to finance its activities without additional subordinated financial support from other parties. FIN 46 applies immediately to variable interest entities created after January 31, 2003, and to variable interest entities in which an enterprise obtains an interest after that date. It applies in the first fiscal year or interim periodperiods beginning after June 15, 2003,2005, and will require the Company to variable interest entities in which an enterprise holds a variable interest thatrecognize compensation cost based on the grant date fair value of the equity instruments it acquired before February 1, 2003.awards. The Company currently accounts for those instruments under the recognition and measurement principles of APB Opinion 25, including the disclosure-only provisions of the original SFAS 123. Accordingly, no compensation cost from issuing equity instruments has not identified and does not expect to identify any variable interest entitiesbeen recognized in the Company's financial statements. The Company estimates that must be consolidated. In December 2002, the Financial Accounting Standards Board issued SFAS 148 "Accounting for Stock-Based Compensation - Transition and Disclosure - an amendment of FASB Statement 123," which is effective for all fiscal years ending after December 15, 2002. SFAS 148 provides alternative methods of transition for a voluntary change to fair value based method of accounting for stock-based employee compensation under SFAS 123 from intrinsic value based method of accounting prescribed by Accounting Principles Board Opinion 25. SFAS 148 also changes the disclosure requirementrequired adoption of SFAS 123 requiring(R) in third quarter 2005 will have a more prominent disclosurenegative impact on its consolidated financial statements. Please see note 1 for an estimate of the pro-forma effect of the fair value based method of accounting for stock-based compensation. The adoption of SFAS 148 by the Company did notimpact this statement would have any impacthad on the Company's consolidated financial statements and is not expected to have any impact on future operations. F-23 net income for the periods covered by this report. F-26