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MEDICAL products beginning with : U
101 to 150 of 933 results  Page: << Previous 50 Results 1 2 [3] 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 >> Next 50 Results
 PRODUCT NAMEFDA Code/Regulation 
Urine Particle Counter (4 suppliers)

Identification. An automated cell counter is a fully-automated or semi-automated device used to count red blood cells, white blood cells, or blood platelets using a sample of the patient's peripheral blood (blood circulating in one of the body's extremities, such as the arm). These devices may also measure hemoglobin or hematocrit and may also calculate or measure one or more of the red cell indices (the erythrocyte mean corpuscular volume, the mean corpuscular hemoglobin, or the mean corpuscular hemoglobin concentration). These devices may use either an electronic particle counting method or an optical counting method.

Classification. Class II (performance standards).

LKM / 864.5200
Urine Screening Kit (40 suppliers)

Identification. A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 866.9.

JXA / 866.2660
Urine Specimen Container for Drugs Of Abuse (14 suppliers)

Identification. An over-the-counter (OTC) test sample collection system for drugs of abuse testing is a device intended to: Collect biological specimens (such as hair, urine, sweat, or saliva), outside of a medical setting and not on order of a health care professional (e.g., in the home, insurance, sports, or workplace setting); maintain the integrity of such specimens during storage and transport in order that the matter contained therein can be tested in a laboratory for the presence of drugs of abuse or their metabolites; and provide access to test results and counseling. This section does not apply to collection, transport, or laboratory testing of biological specimens for the presence of drugs of abuse or their metabolites that is performed to develop evidence for law enforcement purposes.

Classification. Class I (general controls). The device is exempt from the premarket notification requirements in part 807, subpart E of this chapter subject to the limitations in 864.9 if it is sold, distributed, and used in accordance with the restrictions set forth in 809.40 of this chapter. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.198 of this chapter with respect to complaint files.

MPQ / 864.3260
Urine Transport Kit (Excludes Hiv Testing) (3 suppliers)

Identification. A specimen transport and storage container, which may be empty or prefilled, is a device intended to contain biological specimens, body waste, or body exudate during storage and transport in order that the matter contained therein can be destroyed or used effectively for diagnostic examination. If prefilled, the device contains a fixative solution or other general purpose reagent to preserve the condition of a biological specimen added to the container. This section does not apply to specimen transport and storage containers that are intended for use as part of an over-the-counter test sample collection system for drugs of abuse testing.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 864.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180 of this chapter, with respect to general requirements concerning records, and 820.198 of this chapter, with respect to complaint files.

OHZ / 864.3250
Uroflowmeter (29 suppliers)

Identification. A urine flow or volume measuring system is a device that measures directly or indirectly the volume or flow of urine from a patient, either during the course of normal urination or while the patient is catheterized. The device may include a drip chamber to reduce the risk of retrograde bacterial contamination of the bladder and a transducer and electrical signal conditioning and display equipment. This generic type of device includes the electrical urinometer, mechanical urinometer, nonelectric urinometer, disposable nonelectric urine flow rate measuring device, and uroflowmeter.

Classification. (1) Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 876.9.

EXY / 876.1800
Urological Bougie (37 suppliers)

Identification. A urethral dilator is a device that consists of a slender hollow or solid instrument made of metal, plastic, or other suitable material in a cylindrical form and in a range of sizes and flexibilities. The device may include a mechanism to expand the portion of the device in the urethra and indicate the degree of expansion on a dial. It is used to dilate the urethra. This generic type of device includes the mechanical urethral dilator, urological bougies, metal or plastic urethral sound, urethrometer, filiform, and filiform follower.

Classification. (1) Class II (performance standards).

FAX / 876.5520
Urological Catheter and Accessories (6 suppliers)

Identification. A urological catheter and accessories is a flexible tubular device that is inserted through the urethra and used to pass fluids to or from the urinary tract. This generic type of device includes radiopaque urological catheters, ureteral catheters, urethral catheters, coudecatheters, balloon retention type catheters, straight catheters, upper urinary tract catheters, double lumen female urethrographic catheters, disposable ureteral catheters, male urethrographic catheters, and urological catheter accessories including ureteral catheter stylets, ureteral catheter adapters, ureteral catheter holders, ureteral catheter stylets, ureteral catheterization trays, and the gastro-urological irrigation tray (for urological use).

Classification. (1) Class II (performance standards).

MJC / 876.5130
Urological Catheters (61 suppliers)
Urological catheter is a flexible retention catheter. It includes a soft, pliable cone-shaped tip with a reduced urethral contact surface defined by spiral grooves or hair-like projections.

Identification. A urological catheter and accessories is a flexible tubular device that is inserted through the urethra and used to pass fluids to or from the urinary tract. This generic type of device includes radiopaque urological catheters, ureteral catheters, urethral catheters, coudecatheters, balloon retention type catheters, straight catheters, upper urinary tract catheters, double lumen female urethrographic catheters, disposable ureteral catheters, male urethrographic catheters, and urological catheter accessories including ureteral catheter stylets, ureteral catheter adapters, ureteral catheter holders, ureteral catheter stylets, ureteral catheterization trays, and the gastro-urological irrigation tray (for urological use).

Classification. (1) Class II (performance standards).

KOD / 876.5130
Urological Extracorporeal Shock-wave Lithotriptor (15 suppliers)

Identification. An extracorporeal shock wave lithotripter is a device that focuses ultrasonic shock waves into the body to noninvasively fragment urinary calculi within the kidney or ureter. The primary components of the device are a shock wave generator, high voltage generator, control console, imaging/localization system, and patient table. Prior to treatment, the urinary stone is targeted using either an integral or stand-alone localization/imaging system. Shock waves are typically generated using electrostatic spark discharge (spark gap), electromagnetically repelled membranes, or piezoelectric crystal arrays, and focused onto the stone with either a specially designed reflector, dish, or acoustic lens. The shock waves are created under water within the shock wave generator, and are transferred to the patient's body using an appropriate acoustic interface. After the stone has been fragmented by the focused shock waves, the fragments pass out of the body with the patient's urine.

Classification. Class II (special controls) (FDA guidance document: "Guidance for the Content of Premarket Notifications (510(k)'s) for Extracorporeal Shock Wave Lithotripters Indicated for the Fragmentation of Kidney and Ureteral Calculi.")

LNS / 876.5990
Urological Irrigation System (24 suppliers)LJH / 876.5130
Urology Surgical Drapes (159 suppliers)

Identification. A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as to isolate a site of surgical incision from microbial and other contamination. The device includes a plastic wound protector that may adhere to the skin around a surgical incision or be placed in a wound to cover its exposed edges, and a latex drape with a self-retaining finger cot that is intended to allow repeated insertion of the surgeon's finger into the rectum during performance of a transurethral prostatectomy.

Classification. Class II.

KKX / 878.4370
Uroporphyrin Spectrophotometric Test (1 supplier)

Identification. A uroporphyrin test system is a device intended to measure uroporphyrin in urine. Measurements obtained by this device are used in the diagnosis and treatment of porphyrias (primarily inherited diseases associated with disturbed porphyrin metabolism), lead poisoning, and other diseases characterized by alterations in the heme pathway.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 862.9.

JQL / 862.1790
Urosheath Type Incontinence Appliance (23 suppliers)

Identification. A urine collector and accessories is a device intended to collect urine. The device and accessories consist of tubing, a suitable receptacle, connectors, mechanical supports, and may include a means to prevent the backflow of urine or ascent of infection. The two kinds of urine collectors are:

EXJ / 876.5250
Uterine Clamp (43 suppliers)

Identification. An obstetric-gynecologic general manual instrument is one of a group of devices used to perform simple obstetric and gynecologic manipulative functions. This generic type of device consists of the following:

Classification. Class I (general controls). The devices are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 884.9.

HGC / 884.4520
Uterine Curettes (102 suppliers)
Uterine Curettes is a surgical instrument shaped like a scoop or spoon and used to remove tissue or growths from a body cavity. This uterine curette is inserted into the uterine cavity and the wall of the cavity is scraped. The material scraped away from the wall is sending for pathological examination.

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

HCY / 884.4530
Uterine Elevator (14 suppliers)

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

HDP / 884.4530
Uterine Manipulator/Injector Cannula (25 suppliers)LKF / 884.4530
Uterine Packer (12 suppliers)

Identification. An obstetric-gynecologic general manual instrument is one of a group of devices used to perform simple obstetric and gynecologic manipulative functions. This generic type of device consists of the following:

Classification. Class I (general controls). The devices are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 884.9.

HDM / 884.4520
Uterine Sounds (97 suppliers)
Uterine Sounds is used to determine the depth of the uterine cavity. This uterine sound is an endometrial aspirator such as those used for endometrial biopsy sampling. It is used to detect a uterine EMG signal and generate an EMG input signal. It has a bulbous tip to help prevent perforation. It is double-ended, which means that 16 sizes 3-18mm are included.

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

HHM / 884.4530
Uterine Suction Cannula (15 suppliers)

Identification. A vacuum abortion system is a device designed to aspirate transcervically the products of conception or menstruation from the uterus by using a cannula connected to a suction source. This device is used for pregnancy termination or menstrual regulation. This type of device may include aspiration cannula, vacuum source, and vacuum controller.

Classification. Class II (performance standards).

HGH / 884.5070
Uterine Tenaculum (31 suppliers)

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

HDC / 884.4530
Uterotubal Carbon-Dioxide Insufflator and Accessories (8 suppliers)

Identification. A uterotubal carbon dioxide insufflator and accessories is a device used to test the patency (lack of obstruction) of the fallopian tubes by pressurizing the uterus and fallopian tubes and filling them with carbon dioxide gas.

Classification. Class II (performance standards).

HES / 884.1300
Ultraviolet Radiometer (6 suppliers)
Ultraviolet Treatment Cabinet (2 suppliers)
Ultrasonic Bone Cutter (1 supplier)
Unipolar Non-Constrained Elbow Prosthesis (1 supplier)
Upper Body Immobilizer (2 suppliers)
Ultrasonic Vision Aid (2 suppliers)
Uterine Insufflation Cannula (2 suppliers)
Uterine Manipulator Injector & Accessories (8 suppliers)
Uninterruptible (UPS) Power Systems (14 suppliers)
Unit-Dose Drug Delivery System (22 suppliers)
Unit-Dose Liquid Dispenser (7 suppliers)
Unit-Dose Packaging System (9 suppliers)
Universal Dressing (19 suppliers)
Urethane Tubing (10 suppliers)
Urinal Cover (1 supplier)
Urinary Collection Bag (30 suppliers)
Urinary Drainage Unit (12 suppliers)
Used Equipment Service (33 suppliers)
Utensil Washer (5 suppliers)
Utility Glove (12 suppliers)
Urine Cups with Screw Closure (1 supplier)
Urine Cups with Snap Seals (1 supplier)
Urine Cups with Self Adhesive Lid (1 supplier)
Urinometer Jars (2 suppliers)
Urine Teststrips (11 suppliers)
Urine Sediment Tube (2 suppliers)
Urine/Stool Collecting Containers (2 suppliers)
Urological Aprons (2 suppliers)
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