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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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Modulus ALIF Trial Rasp, 8x38x28mm 20° M
Nuvasive, Inc.
1300150
In Commercial Distribution

  • 00195377050649 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 6x38x28mm 20° M
Nuvasive, Inc.
1300149
In Commercial Distribution

  • 00195377050632 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 12x38x28mm 15°
Nuvasive, Inc.
1300148
In Commercial Distribution

  • 00195377050625 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 10x38x28mm 15°
Nuvasive, Inc.
1300147
In Commercial Distribution

  • 00195377050618 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 8x38x28mm 15° M
Nuvasive, Inc.
1300146
In Commercial Distribution

  • 00195377050601 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 6x38x28mm 15° M
Nuvasive, Inc.
1300145
In Commercial Distribution

  • 00195377050595 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 12x38x28mm 10°
Nuvasive, Inc.
1300144
In Commercial Distribution

  • 00195377050588 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 10x38x28mm 10°
Nuvasive, Inc.
1300143
In Commercial Distribution

  • 00195377050571 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 8x38x28mm 10° M
Nuvasive, Inc.
1300142
In Commercial Distribution

  • 00195377050564 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 6x38x28mm 10° M
Nuvasive, Inc.
1300141
In Commercial Distribution

  • 00195377050557 ()


  • Internal spinal fixation procedure kit, reusable
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