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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 Class Implantable

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RELINE-O Screw, 7.0x85mm 2S Monoaxial
Nuvasive, Inc.
13087085
In Commercial Distribution

  • 00887517550774 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x80mm 2S Monoaxial
Nuvasive, Inc.
13087080
In Commercial Distribution

  • 00887517550767 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x75mm 2S Monoaxial
Nuvasive, Inc.
13087075
In Commercial Distribution

  • 00887517550750 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x70mm 2S Monoaxial
Nuvasive, Inc.
13087070
In Commercial Distribution

  • 00887517550743 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x65mm 2S Monoaxial
Nuvasive, Inc.
13087065
In Commercial Distribution

  • 00887517550736 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x60mm 2S Monoaxial
Nuvasive, Inc.
13087060
In Commercial Distribution

  • 00887517550729 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x55mm 2S Monoaxial
Nuvasive, Inc.
13087055
In Commercial Distribution

  • 00887517550712 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x50mm 2S Monoaxial
Nuvasive, Inc.
13087050
In Commercial Distribution

  • 00887517550705 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x45mm 2S Monoaxial
Nuvasive, Inc.
13087045
In Commercial Distribution

  • 00887517550699 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x40mm 2S Monoaxial
Nuvasive, Inc.
13087040
In Commercial Distribution

  • 00887517550682 ()


  • Bone-screw internal spinal fixation system, non-sterile
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