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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 005001 PROGENIX DBM 1CC SRVC FEE
MEDTRONIC SOFAMOR DANEK, INC.
005001
In Commercial Distribution

  • 00613994236418 ()

  • 1 cc volume


  • Bone matrix implant, human-derived
DBM 000505 PRGENIX 0.5CC SRVC FEE
MEDTRONIC SOFAMOR DANEK, INC.
000505
In Commercial Distribution

  • 00613994236401 ()

  • 0.5 cc volume


  • Bone matrix implant, human-derived
DBM 006010 PROGENIX PLUS 10CC
MEDTRONIC SOFAMOR DANEK, INC.
006010
In Commercial Distribution

  • 00613994391049 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
DBM 006005 PROGENIX PLUS 5CC
MEDTRONIC SOFAMOR DANEK, INC.
006005
In Commercial Distribution

  • 00613994391032 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM 006002 PROGENIX PLUS 2.5CC
MEDTRONIC SOFAMOR DANEK, INC.
006002
In Commercial Distribution

  • 00613994391025 ()

  • 2.5 cc volume


  • Bone matrix implant, human-derived
DBM 006001 PROGENIX PLUS 1CC
MEDTRONIC SOFAMOR DANEK, INC.
006001
In Commercial Distribution

  • 00613994391018 ()

  • 1 cc volume


  • Bone matrix implant, human-derived
DBM T44150INT 10CC GRAFTON ORTHOBLEND SM
MEDTRONIC SOFAMOR DANEK, INC.
T44150INT
In Commercial Distribution

  • 00643169134362 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
DBM T44135INT 15CC GRAFTON ORTHOBLEND LG
MEDTRONIC SOFAMOR DANEK, INC.
T44135INT
In Commercial Distribution

  • 00643169134348 ()

  • 15 cc volume


  • Bone matrix implant, human-derived
DBM T44105INT 5CC GRAFTON CRUNCH
MEDTRONIC SOFAMOR DANEK, INC.
T44105INT
In Commercial Distribution

  • 00643169134317 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM T43110 10CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
T43110
In Commercial Distribution

  • 00643169123144 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
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