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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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TRULIANT CC INSRT TOPPER SIZE 2 THIN
Exactech, Inc.
02-029-25-3720
In Commercial Distribution

  • 10885862556912 ()

  • SIZE 2
  • THICK
02-029-25-3720

  • Knee tibia prosthesis trial, reusable
TRULIANT CC INSRT TOPPER SIZE 1 THIN
Exactech, Inc.
02-029-25-3710
In Commercial Distribution

  • 10885862556905 ()

  • THIN
  • SIZE 1
02-029-25-3710

  • Knee tibia prosthesis trial, 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, 80mm C-C Left
Nuvasive, Inc.
Z200282-80
In Commercial Distribution

  • 00195377164063 ()


  • 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, 220mm C-C Left
Nuvasive, Inc.
Z200282-220
In Commercial Distribution

  • 00195377164025 ()


  • 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, 200mm C-C Left
Nuvasive, Inc.
Z200282-200
In Commercial Distribution

  • 00195377164001 ()


  • Internal spinal fixation procedure kit, reusable
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