Surgical Cutter Suppliers
www.biomet.com | Phone: +86-(579)-227-3055
FDA Registration: 3006801265
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Laser Power Probe, Laparoscopic Probes, Guiding Probes, Flexible Depth Gauge (FDA Code: HTJ), ...
Zhejiang Biomet Medical Products Co., Ltd. offers orthopedic and arthritis products. Our Oxford™ partial knee implant is an implant designed to repair only one side of the knee. Our product remo more...
www.ami.at | Send Inquiry | Phone: +43-(5522)-905050
FDA Registration: 3005049530
Products: Surgical Snare (FDA Code: GAE), General & Plastic Surgery Laparoscope (FDA Code: GCJ), Polyglycolic Acid Synthetic Absorbable Suture (FDA Code: GAM), Surgical Cutter (FDA Code: FZT), Ultrasonic Pulsed Doppler Imaging System (FDA Code: IYN), Endoscopic Cleaning Accessories (FDA Code: FEB), ...
Agency For Medical Innovations Gmbh deals with surgical products. Our products are surgical snare, ultrasonic pulsed doppler imaging system and surgical cutter. more...
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.
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 878.9.
