General & Plastic Surgery Surgical Gouge Suppliers
Phone: +1-(514)-739-4010
Products: Wire Cutters (FDA Code: HXZ), Rib Rongeurs (FDA Code: HTX), General & Plastic Surgery Surgical Spatula (FDA Code: GAF), General Surgical Scissors (FDA Code: LRW), Surgical Orthopedic Scissors (FDA Code: HRR), Surgical Pliers (FDA Code: HTC), ...
Bontempi International Inc. focuses on orthopedic products. We provide bone rasps, forceps, cannula, dissectors, hooks, rib rongeurs, surgical scissors and nasal chisels. more...
www.sibelsa.be | Phone: 328-145-0459
Products: Wire Twisters (FDA Code: HXS), Automatic Wire Twisters, Surgical Instruments, Wire Twisters, Sternal Wire Twister, Disposable Electrosurgical Snare, Surgical Snare (FDA Code: GAE), ...
Simal Sa is a manufacturer of surgical instruments. Our products include micro scissors, tissue forceps, hemostatic forceps, clamping forceps, flat and round handle micro needle holders, bulldog & vas 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.
