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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, 5.0x50mm 2S Monoaxial
Nuvasive, Inc.
13085050
In Commercial Distribution

  • 00887517549983 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x45mm 2S Monoaxial
Nuvasive, Inc.
13085045
In Commercial Distribution

  • 00887517549976 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x40mm 2S Monoaxial
Nuvasive, Inc.
13085040
In Commercial Distribution

  • 00887517549969 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x35mm 2S Monoaxial
Nuvasive, Inc.
13085035
In Commercial Distribution

  • 00887517549952 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x30mm 2S Monoaxial
Nuvasive, Inc.
13085030
In Commercial Distribution

  • 00887517549945 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x25mm 2S Monoaxial
Nuvasive, Inc.
13085025
In Commercial Distribution

  • 00887517549938 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x120mm 2S Monoaxial
Nuvasive, Inc.
13085012
In Commercial Distribution

  • 00887517549921 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x110mm 2S Monoaxial
Nuvasive, Inc.
13085011
In Commercial Distribution

  • 00887517549914 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x100mm 2S Monoaxial
Nuvasive, Inc.
13085010
In Commercial Distribution

  • 00887517549907 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.5x95mm 2S Monoaxial
Nuvasive, Inc.
13084595
In Commercial Distribution

  • 00887517549891 ()


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