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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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MAR0FUSE Demineralized Bone Matrix Gel
ARTERIOCYTE MEDICAL SYSTEMS, INC.
MAR0Fuse10cc
Not in Commercial Distribution

  • M896MAR0FUSE10CC1 ()

  • Total Volume: 10 Milliliter


  • Bone matrix implant, human-derived
No Description
Levo Medical Corporation
Manager
In Commercial Distribution

61689

  • Tinnitus masking application software
No Description
Levo Medical Corporation
Patient
In Commercial Distribution

60452

  • Tinnitus masking application software
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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