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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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T-25 HEXALOBE DRIVER
SPINECRAFT, LLC
6000-25
In Commercial Distribution

  • 00193082051241 ()
6000-25

  • General internal orthopaedic fixation system implantation kit
T20 Dedicated Hexalobe Driver
SPINECRAFT, LLC
6000-20-D
In Commercial Distribution

  • 00193082051210 ()
6000-20-D

  • General internal orthopaedic fixation system implantation kit
Universal-Joint Torx driver, T20
SPINECRAFT, LLC
6000-20-J
In Commercial Distribution

  • 00193082051227 ()
6000-20-J

  • General internal orthopaedic fixation system implantation kit
T20 Self-Retaining Driver, No Handle
SPINECRAFT, LLC
6000-20-3-NH
In Commercial Distribution

  • 00193082051203 ()
6000-20-3-NH

  • General internal orthopaedic fixation system implantation kit
T30 Self-retaining Driver with Dedicated Handle
SPINECRAFT, LLC
6000-30-3
In Commercial Distribution

  • 00193082050817 ()
6000-30-3

  • General internal orthopaedic fixation system implantation kit
T20 Self-retaining Driver with Dedicated Handle (optional)
SPINECRAFT, LLC
6000-20-3
In Commercial Distribution

  • 00193082050381 ()
6000-20-3

  • General internal orthopaedic fixation system implantation kit
Closed Ring
ALPHANOX CO.,LTD.
9807-0051
In Commercial Distribution

  • 08806373581632 ()
9807-0051

  • External spinal fixation system
Lordotic Cage Caddy
ALPHANOX CO.,LTD.
9901-5036
In Commercial Distribution

  • 08806373581502 ()
9901-5036

  • Device sterilization/disinfection container, reusable
  • External spinal fixation system
4CIS® Pinehurst Plate Holder
ALPHANOX CO.,LTD.
5932-1114
In Commercial Distribution

  • 08806373581472 ()
5932-1114

  • External spinal fixation system
Ring
ALPHANOX CO.,LTD.
9807-0050
In Commercial Distribution

  • 08806373581243 ()
9807-0050

  • External spinal fixation system
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