Gastroenterologic Needle Holder Suppliers
Phone: +32-(81)-450459
FDA Registration: 3003675041
Products: General use Surgical Curettes (FDA Code: FZS), Surgical Curette (FDA Code: FZS), Non-Powered Surgical Instrument (FDA Code: HAO), Gynecological Fibroid Hook (FDA Code: HDE), Curettes (FDA Code: HTF), Orthopedic Cutting Instrument (FDA Code: HTZ), ...
Surgical Instruments Belgium Sa is a manufacturer of ENT speculum holders, cardiovascular surgical instruments, general & plastic surgery forceps, surgical retractors, surgical retractor systems, nasa more...
Phone: +43-(1)-405-2544
Employee Count: ~10 Quality: ISO 9001, CE Certified
Products: Double Prong Skin Hooks, Bone Rasps (FDA Code: HTR), Intramedullary Bone Rasps, Human Bone Rasps (FDA Code: HTR), Medical Rasps (FDA Code: HTR), Gillies Skin Hook, ...
Alfred Schiller specializes in the repair of dental equipment. more...
www.surgical-access.com | Send Inquiry | Phone: +61-(8)-94186633
Products: Suction Tubes, Stitch Scissors, Standard Suction Tubes, Cardiac Suction Tubes, Surgical Suction Tubes, Nasogastric Suction Tubes, ...
Surgical Access Pty Ltd provides general surgical instruments. We offer instrument repairing services. Our products include of laparoscopy, proctology, intestinal, gall blader, general operating, gyna more...
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.
