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Probes Suppliers

 EMAIL INQUIRY to  221 to 222 of 222 suppliers  Page: << Previous 20 Results 10 11 [12]
Zhejiang Biomet Medical Products Co., Ltd. | Address: No.318, Qiu Tao North Street, Jinhua Industrial Zone, Jinhua, Zhejiang 321016, China China
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...
 
European Footcare Supply | Address: 472 Parkridge Crescent S.E., Calgary, Alberta T2J 5A9, Canada Canada
www.a-foot.com | Send Inquiry | Phone: +403-(271)-6805
FDA Registration: 1000451776
Products: Curettes, Beaver Blades, Bandages, Burs & Drills, AC-Powered Surgical Instrument Motor (FDA Code: GEY), Burr, ...
European Footcare Supply specializes in the production of drill care products, hand instruments and burs. Our drill care products include micro-air, ortho-spray, Erasmus spray and Erasmus mobile drill more...
 EMAIL INQUIRY to  221 to 222 of 222 Probes suppliers  Page: << Previous 20 Results 10 11 [12]
FDA Code / Regulation: HXB / 888.4540

An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.

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 888.9.

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