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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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DBM A44115 15CC GRAFTON CRUNCH
MEDTRONIC SOFAMOR DANEK, INC.
A44115
Not in Commercial Distribution

  • 00613994986146 ()

  • 15 cc volume


  • Bone matrix implant, human-derived
DBM A41110 0.5CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
A41110
Not in Commercial Distribution

  • 00613994986030 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM A41120 1CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
A41120
Not in Commercial Distribution

  • 00613994986023 ()

  • 1 cc volume


  • Bone matrix implant, human-derived
DBM A41130 5CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
A41130
Not in Commercial Distribution

  • 00613994986016 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM A41150 10CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
A41150
Not in Commercial Distribution

  • 00613994986009 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
DBM A43101 0.5CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
A43101
Not in Commercial Distribution

  • 00613994985903 ()

  • 0.5 cc volume


  • Bone matrix implant, human-derived
DBM A43102 1CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
A43102
Not in Commercial Distribution

  • 00613994985897 ()

  • 1 cc volume


  • Bone matrix implant, human-derived
DBM A43103 2.5CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
A43103
Not in Commercial Distribution

  • 00613994985880 ()

  • 2.5 cc volume


  • Bone matrix implant, human-derived
DBM A43105 5CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
A43105
Not in Commercial Distribution

  • 00613994985873 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM A43110 10CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
A43110
Not in Commercial Distribution

  • 00613994985866 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
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