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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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Modulus ALIF Trial Rasp, 12x34x24mm 20°
Nuvasive, Inc.
1300112
In Commercial Distribution

  • 00195377050465 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 10x34x24mm 20°
Nuvasive, Inc.
1300111
In Commercial Distribution

  • 00195377050458 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x34x28mm 20°Sm
Nuvasive, Inc.
1982132
In Commercial Distribution

  • 00195377049421 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x28mm 20°SmDeep
Nuvasive, Inc.
1982131
In Commercial Distribution

  • 00195377049414 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x34x28mm 20°SmDeep
Nuvasive, Inc.
1982130
In Commercial Distribution

  • 00195377049407 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x34x28mm 20°SmDeep
Nuvasive, Inc.
1982129
In Commercial Distribution

  • 00195377049391 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x34x24mm 20°Sm
Nuvasive, Inc.
1982112
In Commercial Distribution

  • 00195377049223 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x24mm 20°Sm
Nuvasive, Inc.
1982111
In Commercial Distribution

  • 00195377049216 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x34x24mm 20°Sm
Nuvasive, Inc.
1982110
In Commercial Distribution

  • 00195377049209 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x34x24mm 20°Sm
Nuvasive, Inc.
1982109
In Commercial Distribution

  • 00195377048899 ()


  • Internal spinal fixation procedure kit, reusable
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