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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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Custom Bone Putty
WRIGHT MEDICAL TECHNOLOGY, INC.
86XC1000
In Commercial Distribution

  • 00840420133519 ()

  • Total Volume: 10 Milliliter
86XC1000

  • Bone matrix implant, human-derived
Custom Bone Putty
WRIGHT MEDICAL TECHNOLOGY, INC.
86XC0500
In Commercial Distribution

  • 00840420133502 ()

  • Total Volume: 5 Milliliter
86XC0500

  • Bone matrix implant, human-derived
DR Graft
WRIGHT MEDICAL TECHNOLOGY, INC.
86DR0300
In Commercial Distribution

  • 00840420133496 ()

  • Total Volume: 3 Milliliter
86DR0300

  • Bone matrix implant, human-derived
RCS Putty w/ CALCIPLEX™ Resorbable Conductive Scaffold
WRIGHT MEDICAL TECHNOLOGY, INC.
86CP0700
In Commercial Distribution

  • 00840420134707 ()

  • Total Volume: 7 Milliliter
86CP0700

  • 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, 3cc
Nuvasive, Inc.
5020403
In Commercial Distribution

  • 00887517971555 ()


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

  • 00887517971548 ()


  • Bone matrix implant, human-derived
Propel DBM Gel Plus, 1cc
Nuvasive, Inc.
5020401
In Commercial Distribution

  • 00887517971531 ()


  • Bone matrix implant, human-derived
Propel DBM Gel, 10cc OUS
Nuvasive, Inc.
5020310994
In Commercial Distribution

  • 00887517971524 ()


  • Bone matrix implant, human-derived
Propel DBM Gel, 10cc
Nuvasive, Inc.
5020310
In Commercial Distribution

  • 00887517971517 ()


  • Bone matrix implant, human-derived
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