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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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BiomaX Bone Graft Putty, 10cc
Surgalign Spine Technologies, Inc.
BMX-0010
In Commercial Distribution

  • 00810076560656 ()

  • 10 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty, 5cc
Surgalign Spine Technologies, Inc.
BMX-0005
In Commercial Distribution

  • 00810076560649 ()

  • 5 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty, 2.5cc
Surgalign Spine Technologies, Inc.
BMX-0002
In Commercial Distribution

  • 00810076560380 ()

  • 2.5 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty, 1cc
Surgalign Spine Technologies, Inc.
BMX-0001
In Commercial Distribution

  • 00810076560007 ()

  • 1 cc


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

  • 00763000140571 ()

  • 10 CC volume


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

  • 00763000140533 ()

  • 10 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
No Description
ShenZhen Antmed Co., Ltd
PT112103
In Commercial Distribution

  • 06945764404104 ()
  • 06945764400403 ()


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

  • 00763000140564 ()

  • 5 CC volume


  • Bone matrix implant, human-derived
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