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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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DBX Putty, 1cc
Musculoskeletal Transplant Foundation, Inc.
038010
In Commercial Distribution

  • W4184038010T0473 ()

  • 1.0 cc volume
038010

  • Bone matrix implant, human-derived
DBX Putty, 0.5cc
Musculoskeletal Transplant Foundation, Inc.
038005
In Commercial Distribution

  • W4184038005T0473 ()

  • 0.5 cc volume
038005

  • Bone matrix implant, human-derived
DBM Putty, 2.5cc
Musculoskeletal Transplant Foundation, Inc.
030025
In Commercial Distribution

  • W4184030025T0473 ()

  • 2.5 cc volume
030025

  • Bone matrix implant, human-derived
DBM Putty, 1.0cc
Musculoskeletal Transplant Foundation, Inc.
030010
In Commercial Distribution

  • W4184030010T0473 ()

  • 1.0 cc volume
030010

  • Bone matrix implant, human-derived
DBM Putty, 0.5cc
Musculoskeletal Transplant Foundation, Inc.
030005
In Commercial Distribution

  • W4184030005T0473 ()

  • 0.5 cc volume
030005

  • Bone matrix implant, human-derived
DBX Paste, 10cc
Musculoskeletal Transplant Foundation, Inc.
028100
In Commercial Distribution

  • W4184028100T0476 ()

  • 10 cc volume
028100

  • Bone matrix implant, human-derived
DBX Paste, 5cc
Musculoskeletal Transplant Foundation, Inc.
028050
In Commercial Distribution

  • W4184028050T0476 ()

  • 5 cc volume
028050

  • Bone matrix implant, human-derived
DBX Paste, 1cc
Musculoskeletal Transplant Foundation, Inc.
028010
In Commercial Distribution

  • W4184028010T0476 ()

  • 1.0 cc volume
028010

  • Bone matrix implant, human-derived
DBX Paste, 0.5cc
Musculoskeletal Transplant Foundation, Inc.
028005
In Commercial Distribution

  • W4184028005T0476 ()
028005

  • 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
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