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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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RELINE-O Screw, 10.5x60mm 2S Monoaxial
Nuvasive, Inc.
13080560
In Commercial Distribution

  • 00887517548566 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x45mm 2S Monoaxial
Nuvasive, Inc.
13080545
In Commercial Distribution

  • 00887517548535 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.5x55mm 2S PLS
Nuvasive, Inc.
13067555
In Commercial Distribution

  • 00887517548375 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.5x45mm 2S PLS
Nuvasive, Inc.
13067545
In Commercial Distribution

  • 00887517548351 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.5x30mm 2S PLS
Nuvasive, Inc.
13067530
In Commercial Distribution

  • 00887517548320 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.5x120mm 2S PLS
Nuvasive, Inc.
13067512
In Commercial Distribution

  • 00887517548306 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.5x110mm 2S PLS
Nuvasive, Inc.
13067511
In Commercial Distribution

  • 00887517548290 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.5x100mm 2S PLS
Nuvasive, Inc.
13067510
In Commercial Distribution

  • 00887517548283 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x90mm 2S PLS
Nuvasive, Inc.
13067090
In Commercial Distribution

  • 00887517548269 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x80mm 2S PLS
Nuvasive, Inc.
13067080
In Commercial Distribution

  • 00887517548245 ()


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