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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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No Description
BIOMET MICROFIXATION, INC
02-3110
In Commercial Distribution

  • 00888233025195 ()
02-3110

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-3105
In Commercial Distribution

  • 00888233025188 ()
02-3105

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-3102
In Commercial Distribution

  • 00888233025171 ()
02-3102

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-3101
In Commercial Distribution

  • 00888233025164 ()
02-3101

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-2905
In Commercial Distribution

  • 00888233025157 ()
02-2905

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-2902
In Commercial Distribution

  • 00888233025140 ()
02-2902

  • 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
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