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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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ADD-A-SWIVEL
Smith & Nephew, Inc.
71031021
In Commercial Distribution

  • 03596010171191 ()
71031021

  • External orthopaedic fixation system, reusable
HEX-FIX UNIVERAL SWIVEL CLAMP
Smith & Nephew, Inc.
71031020
In Commercial Distribution

  • 03596010171184 ()
71031020

  • External orthopaedic fixation system, reusable
HEX-FIX DOUBLE SWIVEL CLAMP
Smith & Nephew, Inc.
71031019
In Commercial Distribution

  • 03596010171177 ()
71031019

  • External orthopaedic fixation system, reusable
HEX-FIX SINGLE SWIVEL CLAMP
Smith & Nephew, Inc.
71031018
In Commercial Distribution

  • 03596010171160 ()
71031018

  • External orthopaedic fixation system, reusable
HEX-FIX DOUBLE PIN CLAMP
Smith & Nephew, Inc.
71031017
In Commercial Distribution

  • 03596010171153 ()
71031017

  • External orthopaedic fixation system, reusable
HEX-FIX SINGLE PIN CLAMP
Smith & Nephew, Inc.
71031016
In Commercial Distribution

  • 03596010171146 ()
71031016

  • External orthopaedic fixation system, reusable
HEX-FIX ADD-A-CLAMP
Smith & Nephew, Inc.
112738
In Commercial Distribution

  • 03596010042507 ()
112738

  • External orthopaedic fixation system, reusable
HEX-FIX METATARSAL PADDLE & CLAMP
Smith & Nephew, Inc.
112709
In Commercial Distribution

  • 03596010042231 ()
112709

  • External orthopaedic fixation system, reusable
SQUARE CONNECT DRIVER SHAFT, T-LIFT
SPINEFRONTIER, INC.
14-05000
In Commercial Distribution

  • 00190361023739 ()


  • Polymeric spinal interbody fusion cage
DRIVER, GEN II INSERTER, SACROFUSE
SPINEFRONTIER, INC.
14-42003
In Commercial Distribution

  • 00190361023647 ()

  • Outer Diameter: 8 Millimeter


  • Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated
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