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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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INSERTER X21520220 15DEG CC 20DE AP LONG
MEDTRONIC SOFAMOR DANEK, INC.
X21520220
In Commercial Distribution

  • 00199150000685 ()


  • Orthopaedic inorganic implant inserter/extractor, reusable
INSERTER X21520180 15DEG CC 20D AP SHORT
MEDTRONIC SOFAMOR DANEK, INC.
X21520180
In Commercial Distribution

  • 00199150000678 ()


  • Orthopaedic inorganic implant inserter/extractor, reusable
XATP MIS Penfield Blade, 80mm C-C Left
Nuvasive, Inc.
Z200282-080
In Commercial Distribution

  • 00195377165855 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 60mm C-C Left
Nuvasive, Inc.
Z200282-060
In Commercial Distribution

  • 00195377165831 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 80mm C-C Right
Nuvasive, Inc.
Z200282-81
In Commercial Distribution

  • 00195377164070 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 60mm C-C Right
Nuvasive, Inc.
Z200282-61
In Commercial Distribution

  • 00195377164056 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 60mm C-C Left
Nuvasive, Inc.
Z200282-60
In Commercial Distribution

  • 00195377164049 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 220mm C-C Right
Nuvasive, Inc.
Z200282-221
In Commercial Distribution

  • 00195377164032 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 200mm C-C Right
Nuvasive, Inc.
Z200282-201
In Commercial Distribution

  • 00195377164018 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 160mm C-C Left
Nuvasive, Inc.
Z200282-160
In Commercial Distribution

  • 00195377163981 ()


  • Internal spinal fixation procedure kit, reusable
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