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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 T43101INT 0.5CC GRAFTON PUTTY
MEDTRONIC SOFAMOR DANEK, INC.
T43101INT
In Commercial Distribution

  • 00643169964969 ()


  • Bone matrix implant, human-derived
DBM T42308INT GRAFTON M PLUGS 8MMX10MM
MEDTRONIC SOFAMOR DANEK, INC.
T42308INT
In Commercial Distribution

  • 00643169964952 ()

  • 8mm x 10mm


  • Bone matrix implant, human-derived
DBM T42275INT 8MMX1CMX10CM 2 EA GRFTON S
MEDTRONIC SOFAMOR DANEK, INC.
T42275INT
In Commercial Distribution

  • 00643169964938 ()


  • Bone matrix implant, human-derived
DBM T45001INT 1CC PASTE GRAFTON PLUS
MEDTRONIC SOFAMOR DANEK, INC.
T45001INT
In Commercial Distribution

  • 00643169965096 ()

  • 1CC


  • Bone matrix implant, human-derived
DBM T43204INT 0.25CC GRAFTON PUTTY SYRNG
MEDTRONIC SOFAMOR DANEK, INC.
T43204INT
In Commercial Distribution

  • 00643169965010 ()


  • Bone matrix implant, human-derived
Tinnitus app Android version 1.0
Widex A/S
Tinnitus app
In Commercial Distribution

  • 05706069674729 ()
5 300 0007 001

  • Tinnitus masking application software
Tinnitus app iOS version 1.0
Widex A/S
Tinnitus app
In Commercial Distribution

  • 05706069674712 ()
5 300 0006 001

  • Tinnitus masking application software
AlloSync CB DBM Putty, 10cc Vial
ISOTIS ORTHOBIOLOGICS, INC.
ABS-2014-10
In Commercial Distribution

  • 10889981153694 ()

  • 10cc
ABS-2014-10

  • Bone matrix implant, human-derived
AlloSync CB DBM Putty, 5cc Vial
ISOTIS ORTHOBIOLOGICS, INC.
ABS-2014-05
In Commercial Distribution

  • 10889981153687 ()

  • 5cc
ABS-2014-05

  • Bone matrix implant, human-derived
OsteoTorrent™ C, Dry DBM Putty with Accell & Cancellous, 2.5cc
Seaspine Orthopedics Corporation
57100025
Not in Commercial Distribution

  • 10889981283940 ()
57100025

  • Bone matrix implant, human-derived
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