Manual Surgical Chisel Suppliers
www.rhosse.com.br | Send Inquiry | Phone: +55-(16)-39659200
Products: Forceps (FDA Code: HTD), Gastroenterologic Needle Holder (FDA Code: FHQ), General & Plastic Surgery Surgical Spatula (FDA Code: GAF), General Surgical Scissors (FDA Code: LRW), Curettes (FDA Code: HTF), ENT Speculum Holder (FDA Code: KAG), ...
Rhosse Instrumentos E Equipamentos Cirurgicos Ltda distributes surgical instruments and equipments. We provide surgical instruments that include open mouth, scissors sharpener, levers, arelotomo, cabe more...
Phone: +011-(6121)-06705360
Products: Forceps (FDA Code: HTD), Bone Hooks (FDA Code: KIK), Scalpel Blade (FDA Code: GES), General Surgical Scissors (FDA Code: LRW), Manual Osteotome (FDA Code: GFI), Manual Surgical Chisel (FDA Code: FZO), ...
Tab Instrumentos Cirurgicos Ltda deals with bone hooks, calipers, curettes and ENT speculum holders. We offer forceps, general & plastic surgery forceps, general & plastic surgery surgical cannula, ge 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.
