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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, 12x38x30mm 30°
Nuvasive, Inc.
1982180
In Commercial Distribution

  • 00195377049902 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 10x38x30mm 30°
Nuvasive, Inc.
1982179
In Commercial Distribution

  • 00195377049896 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 8x38x30mm 30°
Nuvasive, Inc.
1982178
In Commercial Distribution

  • 00195377049889 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 6x38x30mm 30°
Nuvasive, Inc.
1982177
In Commercial Distribution

  • 00195377049872 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 12x38x30mm 25°
Nuvasive, Inc.
1982176
In Commercial Distribution

  • 00195377049865 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 10x38x30mm 25°
Nuvasive, Inc.
1982175
In Commercial Distribution

  • 00195377049858 ()


  • Internal spinal fixation procedure kit, reusable
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
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