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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 in a Lipid Carrier with Porous Calcium Granules
Biomet Orthopedics, LLC
DBMW10
In Commercial Distribution

  • 00888480585251 ()

  • 10 cc
DBMW10

  • Bone matrix implant, human-derived
DBM in a Lipid Carrier with Porous Calcium Granules
Biomet Orthopedics, LLC
DBMW05
In Commercial Distribution

  • 00888480585220 ()

  • 5 cc
DBMW05

  • Bone matrix implant, human-derived
DBM in a Lipid Carrier with Porous Calcium Granules
Biomet Orthopedics, LLC
DBMW02
In Commercial Distribution

  • 00888480585213 ()

  • 2 cc
DBMW02

  • Bone matrix implant, human-derived
Porous Hydroxyapatite Bone Graft Substitute
Biomet Orthopedics, LLC
DBM050
In Commercial Distribution

  • 00888480585206 ()

  • STERILE Granules, 15 cc
DBM050

  • Bone matrix implant, human-derived
Demineralized Bone Matrix (DBM) in a Lipid Carrier
Biomet Orthopedics, LLC
DBM010
In Commercial Distribution

  • 00888480585169 ()

  • 10 cc
DBM010

  • Bone matrix implant, human-derived
Demineralized Bone Matrix (DBM) in a Lipid Carrier
Biomet Orthopedics, LLC
DBM005
In Commercial Distribution

  • 00888480585145 ()

  • 5 cc
DBM005

  • Bone matrix implant, human-derived
Demineralized Bone Matrix (DBM) in a Lipid Carrier
Biomet Orthopedics, LLC
DBM002
In Commercial Distribution

  • 00888480585138 ()

  • 2 cc
DBM002

  • Bone matrix implant, human-derived
Demineralized Bone Matrix (DBM) in a Lipid Carrier
Biomet Orthopedics, LLC
DBM001
In Commercial Distribution

  • 00888480585121 ()

  • 1 cc
DBM001

  • 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
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