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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 P41120 1CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
P41120
Not in Commercial Distribution

  • 00613994985507 ()

  • 1 cc volume


  • Bone matrix implant, human-derived
DBM P41130 5CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
P41130
Not in Commercial Distribution

  • 00613994985491 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM P41150 10CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
P41150
Not in Commercial Distribution

  • 00613994985484 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
DBM T45010 10CC PASTE GRAFTON PLUS
MEDTRONIC SOFAMOR DANEK, INC.
T45010
In Commercial Distribution

  • 00643169123038 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
DBM T45005 5CC PASTE GRAFTON PLUS
MEDTRONIC SOFAMOR DANEK, INC.
T45005
In Commercial Distribution

  • 00643169123021 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM T41150 10CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
T41150
In Commercial Distribution

  • 00643169122987 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
DBM T41130 5CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
T41130
In Commercial Distribution

  • 00643169122970 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM T41120 1CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
T41120
In Commercial Distribution

  • 00643169122963 ()

  • 1 cc volume


  • Bone matrix implant, human-derived
DBM T41110 0.5CC GRAFTON GEL
MEDTRONIC SOFAMOR DANEK, INC.
T41110
In Commercial Distribution

  • 00643169122956 ()

  • 0.5 cc volume


  • Bone matrix implant, human-derived
DBM T45001 1CC PASTE GRAFTON PLUS
MEDTRONIC SOFAMOR DANEK, INC.
T45001
In Commercial Distribution

  • 00643169122949 ()

  • 1 cc volume


  • Bone matrix implant, human-derived
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