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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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AlphaGRAFT, Bone Matrix Gel, Demineralized, 10cc
ALPHATEC SPINE, INC.
1001-100
In Commercial Distribution

  • 00840967111001 ()

  • Total Volume: 10 Milliliter


  • Bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Gel, Demineralized, 1cc
ALPHATEC SPINE, INC.
1001-010
In Commercial Distribution

  • 00840967110998 ()

  • Total Volume: 1 Milliliter


  • Bone matrix implant, human-derived
AlphaGRAFT, Bone Matrix Putty, Demineralized, 10cc
ALPHATEC SPINE, INC.
1002-100
In Commercial Distribution

  • 00840967110981 ()

  • Total Volume: 10 Milliliter


  • Bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.310.1080
In Commercial Distribution

  • D7681031010800 ()

  • .5cc - 5cc
10.310.1080

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.310.1070
In Commercial Distribution

  • D7681031010700 ()

  • .5cc - 5cc
10.310.1070

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.310.1060
In Commercial Distribution

  • D7681031010600 ()

  • .5cc - 5cc
10.310.1060

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.310.1050
In Commercial Distribution

  • D7681031010500 ()

  • .5cc - 5cc
10.310.1050

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.220.1050
In Commercial Distribution

  • D7681022010500 ()

  • .5cc - 5cc
10.220.1050

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.220.1040
In Commercial Distribution

  • D7681022010400 ()

  • .5cc - 5cc
10.220.1040

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.220.1030
In Commercial Distribution

  • D7681022010300 ()

  • .5cc - 5cc
10.220.1030

  • Dental bone matrix implant, human-derived
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