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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 006002 PROGENIX PLUS PUTTY 2.5CC
MEDTRONIC SOFAMOR DANEK, INC.
006002
In Commercial Distribution

  • 00763000140557 ()

  • 2.5 CC volume


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

  • 00763000140540 ()

  • 1 CC volume


  • Bone matrix implant, human-derived
DBM 005110 PROGENIX PUTTY 10CC
MEDTRONIC SOFAMOR DANEK, INC.
005110
In Commercial Distribution

  • 00763000140533 ()

  • 10 CC volume


  • Bone matrix implant, human-derived
DBM 005005 PROGENIX PUTTY 5CC
MEDTRONIC SOFAMOR DANEK, INC.
005005
In Commercial Distribution

  • 00763000140526 ()

  • 5 CC volume


  • Bone matrix implant, human-derived
DBM 005001 PROGENIX PUTTY 1CC
MEDTRONIC SOFAMOR DANEK, INC.
005001
In Commercial Distribution

  • 00763000140519 ()

  • 1 CC volume


  • Bone matrix implant, human-derived
DBM 000505 PROGENIX PUTTY .5CC
MEDTRONIC SOFAMOR DANEK, INC.
000505
In Commercial Distribution

  • 00763000140502 ()

  • 0.5 CC volume


  • Bone matrix implant, human-derived
Propel DBM Gel Plus, 8cc OUS
Nuvasive, Inc.
5020408994
In Commercial Distribution

  • 00887517971586 ()


  • Bone matrix implant, human-derived
Propel DBM Gel Plus, 8cc
Nuvasive, Inc.
5020408
In Commercial Distribution

  • 00887517971579 ()


  • Bone matrix implant, human-derived
Propel DBM Gel Plus, 3cc OUS
Nuvasive, Inc.
5020403994
In Commercial Distribution

  • 00887517971562 ()


  • Bone matrix implant, human-derived
Propel DBM Gel Plus, 1cc OUS
Nuvasive, Inc.
5020401994
In Commercial Distribution

  • 00887517971548 ()


  • Bone matrix implant, human-derived
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