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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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Biomaterials
KEYSTONE DENTAL, INC.
10.110.1060
In Commercial Distribution

  • D7681011010600 ()

  • .5cc - 5cc
10.110.1060

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.110.1050
In Commercial Distribution

  • D7681011010500 ()

  • .5cc - 5cc
10.110.1050

  • Dental bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Putty, Demineralized, 5cc
ALPHATEC SPINE, INC.
1002-050
In Commercial Distribution

  • 00844856026735 ()

  • Total Volume: 5 Milliliter


  • Bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Putty, Demineralized, 2.5cc
ALPHATEC SPINE, INC.
1002-025
In Commercial Distribution

  • 00844856026728 ()

  • Total Volume: 2.5 Milliliter


  • Bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Gel, Demineralized, 5cc
ALPHATEC SPINE, INC.
1001-050
In Commercial Distribution

  • 00844856026711 ()

  • Total Volume: 5 Milliliter


  • Bone matrix implant, human-derived
No Description
Biomet Orthopedics, LLC
406112
In Commercial Distribution

  • 00880304456358 ()

  • 4MM HYBRID(TM) GLENOID TRIAL, SMALL
406112

  • Pure wool pillow
No Description
Biomet Orthopedics, LLC
406114
In Commercial Distribution

  • 00880304456341 ()

  • 4MM HYBRID(TM) GLENOID TRIAL, LARGE
406114

  • Pure wool pillow
No Description
Biomet Orthopedics, LLC
406113
In Commercial Distribution

  • 00880304456334 ()

  • 4MM HYBRID(TM) GLENOID TRIAL, MEDIUM
406113

  • Pure wool pillow
No Description
BIOMET MICROFIXATION, INC
02-3110
In Commercial Distribution

  • 00888233025195 ()
02-3110

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-3105
In Commercial Distribution

  • 00888233025188 ()
02-3105

  • Bone matrix implant, human-derived
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