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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 7509505 MAGNIFUSE II 2.5 CM X 5 CM
MEDTRONIC SOFAMOR DANEK, INC.
7509505
In Commercial Distribution

  • 00643169216235 ()

  • 2.5cm X 5cm


  • Bone matrix implant, human-derived
BONE GRAFT 7509141INT MG 1.75 CM X 10 CM
MEDTRONIC SOFAMOR DANEK, INC.
7509141INT
In Commercial Distribution

  • 00643169141858 ()

  • 1.75cm x 10cm


  • Bone matrix implant, human-derived
DBM T45005INT 5CC PASTE GRAFTON PLUS
MEDTRONIC SOFAMOR DANEK, INC.
T45005INT
In Commercial Distribution

  • 00643169965102 ()


  • Bone matrix implant, human-derived
DBM T45001INT 1CC PASTE GRAFTON PLUS
MEDTRONIC SOFAMOR DANEK, INC.
T45001INT
In Commercial Distribution

  • 00643169965096 ()

  • 1CC


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

  • 00643169965089 ()


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

  • 00643169965065 ()

  • 15cc


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

  • 00643169965010 ()


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

  • 00643169965003 ()

  • 10cc


  • Bone matrix implant, human-derived
DBM T43105INT 5CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
T43105INT
In Commercial Distribution

  • 00643169964990 ()

  • 5CC


  • Bone matrix implant, human-derived
DBM T43103INT 2.5CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
T43103INT
In Commercial Distribution

  • 00643169964983 ()

  • 2.5cc


  • Bone matrix implant, human-derived
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