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Cannula Clamp,Cantor Gastrointestinal Decompression Tube Suppliers & Manufacturers

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Cannula Clamp (FDA Code: FKC / 876.554)

Identification. A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.

Classification. (1) Class III (premarket approval) for the implanted blood access device.

Luxtec, Stryker, Bausch & Lomb, more...

Cantor Gastrointestinal Decompression Tube
Andersen Products, Inc.

Capillary Adapter Cleaning Kit
Hemagen Diagnostics, Inc., Boston Scientific Corporation, Respironics, Inc, more...

Capsule Gastrointestinal Motility System (FDA Code: NYV / 876.1725)
The Smartpill Corporation

Catheter Care Kits
Mentor Corporation, EP Medsystems, Inc., LSL Industries Inc., more...

Catheter Care Tray (FDA Code: OHR / 876.513)

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).

Hollister Incorporated, Rochester Medical Corporation, C. R. Bard, Inc., Bard Medical Div., more...

Catheter Kits With Lube
Catheter kits with lube are a closed system kit that offers less mess, simplifies disposal and decreases the risk of cross-contamination. Each kit contains a catheter, sterile water, lube jelly syringe packaged in plastic tray with peel-back lid, 2 forceps, compartmentalized tray, lubricating catheter channel, specimen container holder and prepping compartment.
Cardinal Health, Inc.

Catheter Plug
ADDTO Inc., Woodhead L.P., Smiths Medical ASD, Inc, more...

Catheter Punch Instrument (FDA Code: FEX / 876.509)

Identification. A suprapubic urological catheter and accessories is a flexible tubular device that is inserted through the abdominal wall into the urinary bladder with the aid of a trocar and cannula. The device is used to pass fluids to and from the urinary tract. This generic type of device includes the suprapubic catheter and tube, Malecot catheter, catheter punch instrument, suprapubic drainage tube, and the suprapubic cannula and trocar.

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

Syneo, Cook Group Incorporated, Aesculap Inc., more...

Catheter Strap
Catheter Strap is designed to reduce accidental dislocation of catheters. It is used around the leg to hold the tubing in place. It is made of two inch wide elastic with loop closure. It helps to provide security against irritation by reducing catheter movement.
Cardinal Health, Inc., Nu-Hope Laboratories, Inc.

Catheterization Kits
Mentor Corporation, Teleflex Medical, DHC Healthcare, more...

Cautery Instruments
Cambrian Medical Inc., Valleylab, Encision Inc., more...

Central Multiple Patient Dialysate Delivery System (FDA Code: FKQ / 876.582)

Identification. A hemodialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and that consists of an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer.

Classification. (1) Class II (performance standards) for hemodialysis systems and all accessories directly associated with the extracorporeal blood system and the dialysate delivery system.

Rismed Oncology Systems, Alden Medical LLC, Minntech Corporation, more...

Chest Drain
Cook Surgical, Inc., Zimmer, Inc., Herger AG, more...

Chest Drain Simulator
Zimmer, Inc., American 3B Scientific, Herger AG, more...

Chest Drain Valve
Cook Surgical, Inc., Zimmer, Inc., Herger AG, more...

Chest Drainage Catheters
Zimmer, Inc., Utah Medical Products, Inc., Rocket Medical, more...

Chest Drainage Unit
Howard Medical Company, Zimmer, Inc., Medela LLC - Healthcare, more...

Chloridimeter
Labconco, Fisher Scientific International, Inc.

Cholecystectomy Kit
Elmed Inc., Conmed Corporation, Ethicon Endo-Surgery, Inc., more...

Chronic Hemodialysis Catheter
Grantadler Corporation, Smiths Medical ASD, Inc, Angiodynamics, Inc., more...

Circular Dermal Biopsy Punch
Elmed Inc., Codman & Shurtleff, Inc., Kmedic, more...

Circumcision Bell (FDA Code: FHG / 884.453)

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).

Hollister Incorporated, Mabis DMI Healthcare, Centurion Medical Products, more...

Classic Closed Tip Urethral Stent Kit
Classic closed tip urethral stent kit contains one classic closed tip ureteral stent and one push catheter.
Gyrus ACMI

Classic Open Tip Urethral Stent Kit
Classic Open Tip Urethral Stent Kit contains one classic open tip ureteral stent with attached braided nylon tether and one push catheter. It features time-tested silicone and tapered-tip design.
Gyrus ACMI

Cleaning Germicide Accessories For Endoscopes (FDA Code: NZA / 876.15)

Identification. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.

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

Steris Corporation

Cleft Palate Prosthesis, Obturators
Innovative Medical Products, Inc, Gyrus ACMI

CLIA-Waived Urine Analyzers
CLIA-waived urine analyzer is designed to perform urine tests. It automatically evaluates the test strip and prints a patient report. This easy-to-use system is an ideal choice for medical practices, small laboratories, or other small-scale testing sites looking to standardize testing and improve efficiency through automated urinalysis testing. It provides immediate and automated documentation of results either as printout or downloaded.
Thermo Fisher Scientific Inc, Becton, Dickson & Co.,

Clinical Extracorporeal Lithotripsy
Elmed Inc., Gyrus ACMI

Closed Tip Ureteral Stent Kit
Cook Group Incorporated, Gyrus ACMI, American Medical Systems, more...

Closed Tip Urethral Stents
Gyrus ACMI, Nidhi Meditech Systems

Closed Urethral Catheterization Trays
Closed urethral catheterization tray contains latex, collection bag, clear vinyl, red rubber, ultrameter, CSR wrap, underpad, nitrile exam gloves, PVP solution, prepping balls, forceps, lubricating jelly and specimen container.
Medtronic, Inc., Rochester Medical Corporation, Cardinal Health, Inc., more...

Closed Urethral Trays
Cardinal Health, Inc.

Coaguloop Resection Electrodes
Gyrus ACMI, C. r. Bard, Inc., Gyrus Group PLC

Coated Implanted Hemodialysis Catheter (FDA Code: NYU / 876.554)

Identification. A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.

Classification. (1) Class III (premarket approval) for the implanted blood access device.

Autosuture, WyMedical Ltd, Davis And Geck Caribe, Ltd.

Coil Canister (FDA Code: FKD / 876.582)

Identification. A hemodialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and that consists of an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer.

Classification. (1) Class II (performance standards) for hemodialysis systems and all accessories directly associated with the extracorporeal blood system and the dialysate delivery system.

Medrad, Inc.

Colon Marker (FDA Code: NBG / 876.15)
PMT Corporation, GI Supply, Mycoscience, Inc.

Colonic Irrigation System (FDA Code: KPL / 876.522)

Identification. A colonic irrigation system is a device intended to instill water into the colon through a nozzle inserted into the rectum to cleanse (evacuate) the contents of the lower colon. The system is designed to allow evacuation of the contents of the colon during the administration of the colonic irrigation. The device consists of a container for fluid connected to the nozzle via tubing and includes a system which enables the pressure, temperature, or flow of water through the nozzle to be controlled. The device may include a console-type toilet and necessary fittings to allow the device to be connected to water and sewer pipes. The device may use electrical power to heat the water. The device does not include the enema kit (876.5210).

Classification. (1) Class II (performance standards) when the device is intended for colon cleansing when medically indicated, such as before radiological or endoscopic examinations.

Diagnostic Automation, Inc., Specialty Health Products, Inc., Progressive Medical Systems, Inc., more...

Color Uroflowmetry System
Laborie Medical Technologies, Menfis Biomedica S.R.L.

Colostomy Appliance
Mentor Corporation, Hollister Incorporated, Cook Group Incorporated, more...

Colostomy Pouch (FDA Code: EZQ / 876.59)

Identification. 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.

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 the limitations in 876.9.

Hollister Incorporated, Stealth Belt Inc., Cymed Ostomy Co., more...

Colostomy Rod (FDA Code: EZP / 876.427)

Identification. A colostomy rod is a device used during the loop colostomy procedure. A loop of colon is surgically brought out through the abdominal wall and the stiff colostomy rod is placed through the loop temporarily to keep the colon from slipping back through the surgical opening.

Classification. Class II (performance standards).

Hollister Incorporated, ConvaTec Inc., Tools for Surgery, LLC, more...

Colostomy Spur Crusher (FDA Code: FHH / 876.473)

Identification. A manual gastroenterology-urology surgical instrument and accessories is a device designed to be used for gastroenterological and urological surgical procedures. The device may be nonpowered, hand-held, or hand-manipulated. Manual gastroenterology-urology surgical instruments include the biopsy forceps cover, biopsy tray without biopsy instruments, line clamp, nonpowered rectal probe, nonelectrical clamp, colostomy spur-crushers, locking device for intestinal clamp, needle holder, gastro-urology hook, gastro-urology probe and director, nonself-retaining retractor, laparotomy rings, nonelectrical snare, rectal specula, bladder neck spreader, self-retaining retractor, and scoop.

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 the limitations in 876.9.

Teleflex Medical, General Surgical Co., (india) Pvt. Ltd., Baur Und Haselbarth-Chirurg Gmbh, more...

Commercial Resection Electrodes
Gyrus ACMI, C. r. Bard, Inc., Gyrus Group PLC

Common Duct Dilators
Codman & Shurtleff, Inc., Himalaya Trading Co. (Pvt) Ltd., Medicon eG

Common Duct Probe
Miltex, Inc., Himalaya Trading Co. (Pvt) Ltd., Bashir, Jamil & Bros. Pvt. Ltd., more...

Compact Cystoscopes
ProEndoscopy, Gyrus ACMI, Stryker, more...

Conditioned Response Enuresis Alarm (FDA Code: KPN / 876.204)

Identification. An enuresis alarm is a device intended for use in treatment of bedwetting. Through an electrical trigger mechanism, the device sounds an alarm when a small quantity of urine is detected on a sensing pad. This generic type of device includes conditioned response enuresis alarms.

Classification. 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.

Enuresis Solutions, LLC, Drynite, Starchild Labs, more...

Condom Urinary Catheter
Professional Products And Services, LLC, S2 Medical Supply, Hollister Incorporated, more...

Continent Colostomy Magnet (FDA Code: KPG)
Applicare Medical Imaging, B.V.

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