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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 Putty, 5cc
ALLOSOURCE
90338005
In Commercial Distribution

  • M536903380051 ()

  • 5 cc
90338005

  • Bone matrix implant, human-derived
AlloFuse® Plus DBM Paste, 3 cc
ALLOSOURCE
90238003
In Commercial Distribution

  • M536902380031 ()

  • 3 cc
90238003

  • 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, 5 cc
ALLOSOURCE
90038005
In Commercial Distribution

  • M536900380051 ()

  • 5 cc
90038005

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

  • M536900380011 ()

  • 1 cc
90038001

  • Bone matrix implant, human-derived
XEMPLIFI DBM Plus, 10cc
GLOBUS MEDICAL, INC.
8103.0210S
In Commercial Distribution

  • 00889095205923 ()

  • Total Volume: 10 Milliliter


  • Bone matrix implant, human-derived
XEMPLIFI DBM Plus, 8cc
GLOBUS MEDICAL, INC.
8103.0208S
In Commercial Distribution

  • 00889095205916 ()

  • Total Volume: 8 Milliliter


  • Bone matrix implant, human-derived
XEMPLIFI DBM Plus, 3cc
GLOBUS MEDICAL, INC.
8103.0203S
In Commercial Distribution

  • 00889095205909 ()

  • Total Volume: 3 Milliliter


  • Bone matrix implant, human-derived
XEMPLIFI DBM Plus, 1cc
GLOBUS MEDICAL, INC.
8103.0201S
In Commercial Distribution

  • 00889095205893 ()

  • Total Volume: 1 Milliliter


  • Bone matrix implant, human-derived
XEMPLIFI DBM Gel, 10cc
GLOBUS MEDICAL, INC.
8103.0110S
In Commercial Distribution

  • 00889095205886 ()

  • Total Volume: 10 Milliliter


  • Bone matrix implant, human-derived
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