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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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HERO DBM PUTTY, 2.5 CC
SPINAL ELEMENTS, INC.
01001-002
In Commercial Distribution

  • 00840606104081 ()


  • Bone matrix implant, human-derived
HERO DBM PUTTY, 1 CC
SPINAL ELEMENTS, INC.
01001-001
In Commercial Distribution

  • 00840606104074 ()


  • Bone matrix implant, human-derived
BEAST PLUS Putty, 10.0cc
Xtant Medical Holdings, Inc.
P01-DBM-3100
In Commercial Distribution

  • 00889795113290 ()


  • Bone matrix implant, human-derived
BEAST PLUS Putty, 5.0cc
Xtant Medical Holdings, Inc.
P01-DBM-3050
In Commercial Distribution

  • 00889795113283 ()


  • Bone matrix implant, human-derived
BEAST PLUS Putty, 2.5cc
Xtant Medical Holdings, Inc.
P01-DBM-3025
In Commercial Distribution

  • 00889795113276 ()


  • Bone matrix implant, human-derived
BEAST Injectable Putty, 10cc
Xtant Medical Holdings, Inc.
P01-DBM-2100
In Commercial Distribution

  • 00889795113269 ()


  • Bone matrix implant, human-derived
BEAST Injectable Putty, 5.0cc
Xtant Medical Holdings, Inc.
P01-DBM-2050
In Commercial Distribution

  • 00889795113252 ()


  • Bone matrix implant, human-derived
BEAST Injectable Putty, 2.5cc
Xtant Medical Holdings, Inc.
P01-DBM-2025
In Commercial Distribution

  • 00889795113245 ()


  • Bone matrix implant, human-derived
BEAST Injectable Putty, 1.0cc
Xtant Medical Holdings, Inc.
P01-DBM-2010
In Commercial Distribution

  • 00889795113238 ()


  • Bone matrix implant, human-derived
Power Mix
WRIGHT MEDICAL TECHNOLOGY, INC.
876P0200
In Commercial Distribution

  • 00889797076036 ()

  • Total Volume: 20 Milliliter
876P0200

  • Bone matrix implant, human-derived
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