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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 T43205INT 0.5CC GRAFTON PUTTY SYRNG
MEDTRONIC SOFAMOR DANEK, INC.
T43205INT
In Commercial Distribution

  • 00643169134300 ()

  • 0.5cc


  • Bone matrix implant, human-derived
DBM T43204INT 0.25CC GRAFTON PUTTY SYRNG
MEDTRONIC SOFAMOR DANEK, INC.
T43204INT
In Commercial Distribution

  • 00643169134294 ()

  • 0.25cc


  • Bone matrix implant, human-derived
DBM T43110INT 10CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
T43110INT
In Commercial Distribution

  • 00643169134287 ()

  • 10cc


  • Bone matrix implant, human-derived
DBM T43102 1CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
T43102
In Commercial Distribution

  • 00643169123175 ()

  • 1cc volume


  • Bone matrix implant, human-derived
DBM T43103 2.5CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
T43103
In Commercial Distribution

  • 00643169123168 ()

  • 2.5cc volume


  • Bone matrix implant, human-derived
DBM T43105 5CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
T43105
In Commercial Distribution

  • 00643169123151 ()

  • 5cc 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
DBM T43204 0.25CC GRAFTON PUTTY SYRINGE
MEDTRONIC SOFAMOR DANEK, INC.
T43204
In Commercial Distribution

  • 00643169123137 ()

  • 0.25cc volume


  • Bone matrix implant, human-derived
DBM T44105 5CC GRAFTON CRUNCH
MEDTRONIC SOFAMOR DANEK, INC.
T44105
In Commercial Distribution

  • 00643169123120 ()

  • 5cc volume


  • Bone matrix implant, human-derived
DBM T44115 15CC GRAFTON CRUNCH
MEDTRONIC SOFAMOR DANEK, INC.
T44115
In Commercial Distribution

  • 00643169123113 ()

  • 15cc volume


  • Bone matrix implant, human-derived
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