Rectal Catheter for Continent Ileostomy Suppliers
EMAIL INQUIRY to 5 suppliers
Zassi Medical Evolutions, Inc. | Address: 1886 S. 14th St., Suite 6, Fernandina Beach, Florida 32034, USA 
www.zassimedical.com | Send Inquiry | Phone: +1-(904)-261-2169
Year Established: 1997 Annual Revenues: USD 1-5 Million Quality: ISO, CE Certified
Products: Rectal Catheter for Continent Ileostomy (FDA Code: KPH), ...
Zassi Medical Evolutions, Inc. is a medical device company specializing in gastrointestinal products for waste management and continence control. Our continent ostomy system includes a family of singl more...
www.zassimedical.com | Send Inquiry | Phone: +1-(904)-261-2169
Year Established: 1997 Annual Revenues: USD 1-5 Million Quality: ISO, CE Certified
Products: Rectal Catheter for Continent Ileostomy (FDA Code: KPH), ...
Zassi Medical Evolutions, Inc. is a medical device company specializing in gastrointestinal products for waste management and continence control. Our continent ostomy system includes a family of singl more...
Rece International Corp. | Address: 5881 N.W. 151st St., Ste. 111, Miami Lakes, Florida 33014, USA
Phone: +1-(305)-3626555
FDA Registration: 3003965134
Products: Oxygen Masks (FDA Code: BYG), Gastroenterologic Needle Holder (FDA Code: FHQ), Urine Collection Leg Bags (FDA Code: FAQ), Tongue Depressors (FDA Code: FMA), Infusion Catheter (FDA Code: JCY), Elastic Bandages (FDA Code: FQM), ...
Rece International Corp. provides surgical and medical equipments such as adult tongue depressors, blood collection lancets, elastic stockings, emesis basins, hydrophilic wound dressings, venturi low more...
Phone: +1-(305)-3626555
FDA Registration: 3003965134
Products: Oxygen Masks (FDA Code: BYG), Gastroenterologic Needle Holder (FDA Code: FHQ), Urine Collection Leg Bags (FDA Code: FAQ), Tongue Depressors (FDA Code: FMA), Infusion Catheter (FDA Code: JCY), Elastic Bandages (FDA Code: FQM), ...
Rece International Corp. provides surgical and medical equipments such as adult tongue depressors, blood collection lancets, elastic stockings, emesis basins, hydrophilic wound dressings, venturi low more...
Astra Tech Ab | Address: Box 14 Aminogatan 1, Molndal 43121, Sweden
www.astratech.com | Phone: 31/776-3000
FDA Registration: 9612468 Annual Revenues: USD 100-500 Million Employee Count: ~600 Quality: ISO 9001, CE Certified
Products: Urethral Catheters (FDA Code: GBM), Urinary Catheters, Urological Catheters (FDA Code: KOD), Ultrasonic Surgical Aspirator, Miniature Ultrasonic Surgical Aspirator, Surgical Aspirator, ...
Astra Tech Ab is a manufacturer of health care devices and dental implants. more...
www.astratech.com | Phone: 31/776-3000
FDA Registration: 9612468 Annual Revenues: USD 100-500 Million Employee Count: ~600 Quality: ISO 9001, CE Certified
Products: Urethral Catheters (FDA Code: GBM), Urinary Catheters, Urological Catheters (FDA Code: KOD), Ultrasonic Surgical Aspirator, Miniature Ultrasonic Surgical Aspirator, Surgical Aspirator, ...
Astra Tech Ab is a manufacturer of health care devices and dental implants. more...
General Surgical Co., (india) Pvt. Ltd. | Address: G-6 Gee Cee Crescent, 114, Ponamallee High Road, Chennai, Tamil Nadu 60084, India 
www.gescoindia.com | Send Inquiry | Phone: +91-(44)-2825 96 02
FDA Registration: 9613926 Quality: ISO 9001:2000 Certified
Products: Vaginal Retractors (FDA Code: HDL), Forceps (FDA Code: HTD), Probes (FDA Code: HXB), Saws (FDA Code: HSO), Surgical Marking Pens (FDA Code: HRP), Gastroenterologic Needle Holder (FDA Code: FHQ), ...
General Surgical Co., (india) Pvt. Ltd. is a manufacturer of surgical instruments. We produce medical & surgical disposables, general, ENT, neuro & spinal, orthopedic, gynecology & obstetrics, plastic more...
www.gescoindia.com | Send Inquiry | Phone: +91-(44)-2825 96 02
FDA Registration: 9613926 Quality: ISO 9001:2000 Certified
Products: Vaginal Retractors (FDA Code: HDL), Forceps (FDA Code: HTD), Probes (FDA Code: HXB), Saws (FDA Code: HSO), Surgical Marking Pens (FDA Code: HRP), Gastroenterologic Needle Holder (FDA Code: FHQ), ...
General Surgical Co., (india) Pvt. Ltd. is a manufacturer of surgical instruments. We produce medical & surgical disposables, general, ENT, neuro & spinal, orthopedic, gynecology & obstetrics, plastic more...
Coloplast A/S | Address: Holtedam 1, Humlebaek DK-3050, Denmark
www.coloplast.com | Send Inquiry | Phone: +45-(0)-4911-1111
FDA Registration: 9610694 Year Established: 1957 Annual Revenues: USD 100-500 Million Employee Count: ~7000 Quality: CE Certified
Products: Urethral Catheters (FDA Code: GBM), Urine Collection Leg Bags (FDA Code: FAQ), Straight Catheter (FDA Code: EZD), Urological Catheters (FDA Code: KOD), Penile Prosthesis (FDA Code: FAE), Sterile Leg Urine Collection Bag for External Use (FDA Code: FAQ), ...
Coloplast A/S develops products and services that make life easier for people with very personal & private medical conditions. Our business includes ostomy care, urology & continence care, and wound & more...
www.coloplast.com | Send Inquiry | Phone: +45-(0)-4911-1111
FDA Registration: 9610694 Year Established: 1957 Annual Revenues: USD 100-500 Million Employee Count: ~7000 Quality: CE Certified
Products: Urethral Catheters (FDA Code: GBM), Urine Collection Leg Bags (FDA Code: FAQ), Straight Catheter (FDA Code: EZD), Urological Catheters (FDA Code: KOD), Penile Prosthesis (FDA Code: FAE), Sterile Leg Urine Collection Bag for External Use (FDA Code: FAQ), ...
Coloplast A/S develops products and services that make life easier for people with very personal & private medical conditions. Our business includes ostomy care, urology & continence care, and wound & more...
EMAIL INQUIRY to 5 Rectal Catheter for Continent Ileostomy suppliers
FDA Code / Regulation: KPH / 876.5030
A continent ileostomy catheter is a flexible tubular device used as a form during surgery for continent ileostomy and it provides drainage after surgery. Additionally, the device may be inserted periodically by the patient for routine care to empty the ileal pouch. This generic type of device includes the rectal catheter for continent ileostomy.
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.
