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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 HL Trial, 8x38x30mm 25°
Nuvasive, Inc.
1982174
In Commercial Distribution

  • 00195377049841 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 6x38x30mm 25°
Nuvasive, Inc.
1982173
In Commercial Distribution

  • 00195377049834 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x38x30mm 20°Med
Nuvasive, Inc.
1982172
In Commercial Distribution

  • 00195377049827 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x30mm 20°Med
Nuvasive, Inc.
1982171
In Commercial Distribution

  • 00195377049810 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x38x30mm 20°Med
Nuvasive, Inc.
1982170
In Commercial Distribution

  • 00195377049803 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x38x30mm 20°Med
Nuvasive, Inc.
1982169
In Commercial Distribution

  • 00195377049797 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x38x30mm 15°Med
Nuvasive, Inc.
1982168
In Commercial Distribution

  • 00195377049780 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x30mm 15°Med
Nuvasive, Inc.
1982167
In Commercial Distribution

  • 00195377049773 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x38x30mm 15°Med
Nuvasive, Inc.
1982166
In Commercial Distribution

  • 00195377049766 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x38x30mm 15°Med
Nuvasive, Inc.
1982165
In Commercial Distribution

  • 00195377049759 ()


  • Internal spinal fixation procedure kit, reusable
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