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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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DEMINERALIZED BONE MATRIX (DMB) 2.0CC
BIOMET 3I, LLC
ROAP20
In Commercial Distribution

  • 00844868035510 ()

  • Volume 2 mL


  • Dental bone matrix implant, human-derived
DEMINERALIZED BONE MATRIX (DMB) 1.0CC
BIOMET 3I, LLC
ROAP10
In Commercial Distribution

  • 00844868035503 ()

  • Volume 1 mL


  • Dental 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
AlphaGRAFT, Bone Matrix Gel, Demineralized, 5cc
ALPHATEC SPINE, INC.
1001-050
In Commercial Distribution

  • 00844856026711 ()

  • Total Volume: 5 Milliliter


  • Bone matrix implant, human-derived
No Description
Sound Options Tinnitus Treatments Inc
2.0
In Commercial Distribution

  • 00627843723226 ()


  • Tinnitus masking application software
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