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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 Paste
Rti Surgical, Inc.
005710
In Commercial Distribution

  • 00854095006306 ()
005710

  • Bone matrix implant, human-derived
DBM Paste
Rti Surgical, Inc.
005705
In Commercial Distribution

  • 00854095006290 ()
005705

  • Bone matrix implant, human-derived
DBM Paste
Rti Surgical, Inc.
005701
In Commercial Distribution

  • 00854095006283 ()
005701

  • Bone matrix implant, human-derived
DBM Paste
Rti Surgical, Inc.
005700
In Commercial Distribution

  • 00854095006276 ()
005700

  • Bone matrix implant, human-derived
DBM 006010 PROGENIX PLUS 10CC
MEDTRONIC SOFAMOR DANEK, INC.
006010
In Commercial Distribution

  • 00613994391049 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
DBM 006005 PROGENIX PLUS 5CC
MEDTRONIC SOFAMOR DANEK, INC.
006005
In Commercial Distribution

  • 00613994391032 ()

  • 5 cc volume


  • Bone matrix implant, human-derived
DBM 006001 PROGENIX PLUS 1CC
MEDTRONIC SOFAMOR DANEK, INC.
006001
In Commercial Distribution

  • 00613994391018 ()

  • 1 cc volume


  • Bone matrix implant, human-derived
DBM 006002 PROGENIX PLUS 2.5CC
MEDTRONIC SOFAMOR DANEK, INC.
006002
In Commercial Distribution

  • 00613994391025 ()

  • 2.5 cc volume


  • Bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Putty, Demineralized, 5cc
ALPHATEC SPINE, INC.
1002-050
In Commercial Distribution

  • 00844856026735 ()

  • Total Volume: 5 Milliliter


  • Bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Putty, Demineralized, 2.5cc
ALPHATEC SPINE, INC.
1002-025
In Commercial Distribution

  • 00844856026728 ()

  • Total Volume: 2.5 Milliliter


  • Bone matrix implant, human-derived
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