Profile: Cook Group Incorporated focuses on the research and product development in minimally invasive medical device technology for diagnostic & therapeutic procedures. Our wire-guided arndt endobronchial blocker set allows one-lung ventilation using a conventional endotrachael tube and a pediatric fiberoptic bronchoscope. Our central venous catheter sets & trays are used for venous pressure monitoring, blood sampling and administration of drugs & fluids.

The company has ~340 employees and is ISO 9000, CE certified.

FDA Registration Number: 1820334

301 to 338 of 338 Products/Services (Click for related suppliers)  Page: 1 2 3 4 5 6 [7]

• Tube Introduction Forceps (FDA Code: BWB / 868.5780) Tube introduction forceps (e.g., Magill forceps) are a right-angled device used to grasp a tracheal tube and place it in a patient's trachea.

• Tumor Localization Needle (FDA Code: MIJ / 878.4800) A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.

• Tungsten Carbide Needle Holders

• Ultra Stiff Wire Guides

• Upper Urinary Tract Catheter (FDA Code: EYC / 876.5130) 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).

• Ureteral Catheter Adapter (FDA Code: EYI / 876.5130)

• Ureteral Catheter Dilator (FDA Code: EZN / 876.5470) A ureteral dilator is a device that consists of a specially shaped catheter or bougie and is used to dilate the ureter at the place where a stone has become lodged or to dilate a ureteral stricture.

• Ureteral Disposable Catheter (FDA Code: FGF / 876.5130)

• Ureteral Splint (FDA Code: FAD / 876.4620) A ureteral stent is a tube-like implanted device that is inserted into the ureter to provide ureteral rigidity and allow the passage of urine. The device may have finger-like protrusions or hooked ends to keep the tube in place. It is used in the treatment of ureteral injuries and ureteral obstruction.

• Ureteral Stent

• Ureteroscopic Biopsy Forceps

• Ureterostomy Urinary Collection Bag (FDA Code: EXG / 876.5900) An ostomy pouch and accessories is a device that consists of a bag that is attached to the patient's skin by an adhesive material and that is intended for use as a receptacle for collection of fecal material or urine following an ileostomy, colostomy, or ureterostomy (a surgically created opening of the small intestine, large intestine, or the ureter on the surface of the body). This generic type of device and its accessories includes the ostomy pouch, ostomy adhesive, the disposable colostomy appliance, ostomy collector, colostomy pouch, urinary ileostomy bag, urine collecting ureterostomy bag, ostomy drainage bag with adhesive, stomal bag, ostomy protector, and the ostomy size selector, but excludes ostomy pouches which incorporate arsenic-containing compounds.

• Urethral Catheters (FDA Code: GBM / 876.5130)

• Urethral Dilator Set and Dilators

• Urethral Dilators (FDA Code: KOE / 876.5520) 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.

• Urethrogram Catheters

• Urodynamics Catheters

• Urological Catheter Care Kits

• Urological Catheters (FDA Code: KOD / 876.5130)

• Urological Catheters, Intermittent Catheters

• Urological Percutaneous Pigtail Nephrostomy Sets

• Urological Stone Manipulation Devices, Pediatric

• Uterine Biopsy Forceps

• Uterine Sound Devices

• Uterine Sound Instruments

• Uterine Sounds (FDA Code: HHM / 884.4530) 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:

• Vacuum Collection Bottle (FDA Code: KDQ / 880.6740) A vacuum-powered body fluid suction apparatus is a device used to aspirate, remove, or sample body fluids. The device is powered by an external source of vacuum. This generic type of device includes vacuum regulators, vacuum collection bottles, suction catheters and tips, connecting flexible aspirating tubes, rigid suction tips, specimen traps, noninvasive tubing, and suction regulators (with gauge).

• Vascular Access Graft (FDA Code: LTH)

• Vascular Device for Promoting Embolization (FDA Code: KRD / 870.3300)

• Vascular Needle Holder

• Vena Cava Filters

• Ventricular (Containing Antibiotic Or Antimicrobial Agents) Catheter (FDA Code: NHC / 882.4100) A ventricular catheter is a device used to gain access to the cavities of the brain for injection of material into, or removal of material from, the brain.

• Vertebroplasty Bone Cement (FDA Code: NDN / 888.3027) Polymethylmethacrylate (PMMA) bone cement is a device intended to be implanted that is made from methylmethacrylate, polymethylmethacrylate, esters of methacrylic acid, or copolymers containing polymethylmethacrylate and polystyrene. The device is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.

• Vertebroplasty Sets

• Vertical Needle Holder

• Vessel Dilatation Balloon Catheter

• Vessel Harvesting Tools

• Weatherproof First Aid Kit