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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® 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
AlphaGRAFT, Bone Matrix Gel, Demineralized, 10cc
ALPHATEC SPINE, INC.
1001-100
In Commercial Distribution

  • 00840967111001 ()

  • Total Volume: 10 Milliliter


  • Bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Gel, Demineralized, 1cc
ALPHATEC SPINE, INC.
1001-010
In Commercial Distribution

  • 00840967110998 ()

  • Total Volume: 1 Milliliter


  • Bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Putty, Demineralized, 10cc
ALPHATEC SPINE, INC.
1002-100
In Commercial Distribution

  • 00840967110981 ()

  • Total Volume: 10 Milliliter


  • Bone matrix implant, human-derived
HERO DBM+ PUTTY, 10CC
SPINAL ELEMENTS, INC.
01004-010
In Commercial Distribution

  • 00840606104180 ()


  • Bone matrix implant, human-derived
HERO DBM+ PUTTY, 5CC
SPINAL ELEMENTS, INC.
01004-005
In Commercial Distribution

  • 00840606104173 ()


  • Bone matrix implant, human-derived
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