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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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XATP MIS Penfield Blade, 160mm C-C Right
Nuvasive, Inc.
Z200282-161
In Commercial Distribution

  • 00195377163998 ()


  • 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
XATP MIS Penfield Blade, 140mm C-C Right
Nuvasive, Inc.
Z200282-141
In Commercial Distribution

  • 00195377163974 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 140mm C-C Left
Nuvasive, Inc.
Z200282-140
In Commercial Distribution

  • 00195377163967 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 100mm C-C Right
Nuvasive, Inc.
Z200282-101
In Commercial Distribution

  • 00195377163950 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 100mm C-C Left
Nuvasive, Inc.
Z200282-100
In Commercial Distribution

  • 00195377163943 ()


  • Internal spinal fixation procedure kit, reusable
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
TRULIANT CC INSRT TOPPER SIZE 5 THICK
Exactech, Inc.
02-029-25-3850
In Commercial Distribution

  • 10885862556998 ()

  • SIZE 5
  • THICK
02-029-25-3850

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 4 THICK
Exactech, Inc.
02-029-25-3840
In Commercial Distribution

  • 10885862556981 ()

  • SIZE 4
  • THICK
02-029-25-3840

  • Knee tibia prosthesis trial, reusable
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