Surgical Retainer Suppliers
www.xinhuasurgical.com | Phone: +86-(0533)-3595351
FDA Registration: 3005440795
Products: Saws (FDA Code: HSO), General & Plastic Saw Surgical Blade (FDA Code: GFA), Drill Handpiece (Brace) (FDA Code: HBD), Surgical Knife (FDA Code: EMF), Neurosurgical Suture Needle (FDA Code: HAS), Gynecological Cerclage Needle (FDA Code: HDH), ...
Xinhua Surgical Instrument Company Ltd. manufactures surgical instruments. Our products include dental instruments, veterinary instruments, sterilizers, autoclaves and dressing containers, electric su more...
www.wandara.com | Send Inquiry | Phone: +61-(3)-98709592
Products: General Surgical Aids, Surgical Sterilizing Aids, Abdominal Retractor, Abdominal Supports, Abdominal Surgery Instrument, Surgical Retainer (FDA Code: GCZ), ...
Wandara Pty Ltd is a manufacturer of murray cod to assist with abdominal closures. Our murray cod is manufactured using surgical grade silicon, and it acts as a visceral guard. It is introduced into t 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.
