SEARCH RESULTS FOR: (*Forged New Hampshire driver*)(572533 results)

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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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No Description
Osstem Implant Co., Ltd.
HKSNMDCRE
In Commercial Distribution

  • 08800209374801 ()


  • Surgical screwdriver, reusable
No Description
Osstem Implant Co., Ltd.
HKSFDL
In Commercial Distribution

  • 08800209374788 ()


  • Surgical screwdriver, reusable
SCREWDRIVER SHAFT HEX 2.5MM SELF-HOLD L 300MM FOR QC
Synthes GmbH
03.164.024
In Commercial Distribution

  • 07612334216779 ()
  • 10886982311115 ()
03164024

  • Surgical screwdriver, reusable
SCREWDRIVER STARDRIVE® 3.5 T15 LENGTH 365 MM
Synthes GmbH
03.164.027
In Commercial Distribution

  • 07612334216809 ()
  • 10886982311092 ()
03164027

  • Surgical screwdriver, reusable
SCREWDRIVER HEXAGONAL 2.5MM SELF-HOLDING L 365MM
Synthes GmbH
03.164.026
In Commercial Distribution

  • 07612334216793 ()
  • 10886982311085 ()
03164026

  • Surgical screwdriver, reusable
SCREWDRIVER SHAFT STARDRIVE® 3.5 T15 LENGTH 300 MM FOR QC
Synthes GmbH
03.164.025
In Commercial Distribution

  • 07612334216786 ()
  • 10886982311078 ()
03164025

  • Surgical screwdriver, reusable
Coverplate Driver
KYOCERA MEDICAL TECHNOLOGIES, INC.
Tesera-k ALIF
In Commercial Distribution

  • 00841523156078 ()
2167-003-005

  • General internal orthopaedic fixation system implantation kit
Retaining Hex Driver
KYOCERA MEDICAL TECHNOLOGIES, INC.
Tesera-k ALIF
In Commercial Distribution

  • 00841523156030 ()
2167-002-015

  • General internal orthopaedic fixation system implantation kit
U-Jointed Hex Driver - SG
KYOCERA MEDICAL TECHNOLOGIES, INC.
Tesera-k ALIF
In Commercial Distribution

  • 00841523155989 ()
2167-002-010

  • General internal orthopaedic fixation system implantation kit
U-Jointed Hex Driver
KYOCERA MEDICAL TECHNOLOGIES, INC.
Tesera-k ALIF
In Commercial Distribution

  • 00841523155972 ()
2167-002-009

  • General internal orthopaedic fixation system implantation kit
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