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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 Class Implantable

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RELINE-C Bender Tip, Ø4.0 Ang Sag Left
Nuvasive, Inc.
3790053
In Commercial Distribution

  • 00887517006103 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-C Bender Tip, Ø3.5 Ang Sag Left
Nuvasive, Inc.
3790052
In Commercial Distribution

  • 00887517006097 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-C Bender Tip, Ø4.0 Str Sagittal
Nuvasive, Inc.
3790051
In Commercial Distribution

  • 00887517006080 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-C Bender Tip, Ø4.0 Ang Sagittal R
Nuvasive, Inc.
3790050
In Commercial Distribution

  • 00887517006073 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-C Bender Tip, Ø3.5 Str Sagittal
Nuvasive, Inc.
3790049
In Commercial Distribution

  • 00887517006066 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-C Bender Tip, Ø3.5 Ang Sagittal R
Nuvasive, Inc.
3790048
In Commercial Distribution

  • 00887517006059 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-C Driver, Hex
Nuvasive, Inc.
3790047
In Commercial Distribution

  • 00887517006042 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-C Handle, Small Ratcheting
Nuvasive, Inc.
3790046
In Commercial Distribution

  • 00887517006035 ()


  • Surgical instrument handle, non-torque-limiting
RELINE-C Guide, 12-14mm Occip Drill/Tap
Nuvasive, Inc.
3790045
In Commercial Distribution

  • 00887517006028 ()


  • Internal spinal fixation procedure kit, reusable
RRELINE-C Bender 2, Cross-Connecter
Nuvasive, Inc.
3790044
In Commercial Distribution

  • 00887517006011 ()


  • Internal spinal fixation procedure kit, reusable
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