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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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AlloFuse® Plus DBM Paste, 1 cc
ALLOSOURCE
90238001
In Commercial Distribution

  • M536902380011 ()

  • 1 cc
90238001

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 10cc
ALLOSOURCE
90138010
In Commercial Distribution

  • M536901380101 ()

  • 10 cc
90138010

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 5 cc
ALLOSOURCE
90138005
In Commercial Distribution

  • M536901380051 ()

  • 5 cc
90138005

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 1 cc
ALLOSOURCE
90138001
In Commercial Distribution

  • M536901380011 ()

  • 1 cc
90138001

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 10 cc
ALLOSOURCE
90038010
In Commercial Distribution

  • M536900380101 ()

  • 10 cc
90038010

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 5 cc
ALLOSOURCE
90038005
In Commercial Distribution

  • M536900380051 ()

  • 5 cc
90038005

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 2.5 cc
ALLOSOURCE
90038002
In Commercial Distribution

  • M536900380021 ()

  • 2.5 cc
90038002

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 1 cc
ALLOSOURCE
90038001
In Commercial Distribution

  • M536900380011 ()

  • 1 cc
90038001

  • Bone matrix implant, human-derived
MAR0Fuse Demineralized Bone Matrix Gel
ARTERIOCYTE MEDICAL SYSTEMS, INC.
MAR0Fuse5cc
Not in Commercial Distribution

  • M896MAR0FUSE5CC1 ()

  • Total Volume: 5 Milliliter


  • Bone matrix implant, human-derived
MAR0Fuse Demineralized Bone Matrix Gel
ARTERIOCYTE MEDICAL SYSTEMS, INC.
MAR0Fuse1cc
Not in Commercial Distribution

  • M896MAR0FUSE1CC1 ()

  • Total Volume: 1 Milliliter


  • Bone matrix implant, human-derived
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