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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, 5.5x45mm 2S Monoaxial
Nuvasive, Inc.
13085545
In Commercial Distribution

  • 00887517550156 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.5x35mm 2S Monoaxial
Nuvasive, Inc.
13085535
In Commercial Distribution

  • 00887517550132 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.5x120mm 2S Monoaxial
Nuvasive, Inc.
13085512
In Commercial Distribution

  • 00887517550101 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.5x100mm 2S Monoaxial
Nuvasive, Inc.
13085510
In Commercial Distribution

  • 00887517550088 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x95mm 2S Monoaxial
Nuvasive, Inc.
13085095
In Commercial Distribution

  • 00887517550071 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x85mm 2S Monoaxial
Nuvasive, Inc.
13085085
In Commercial Distribution

  • 00887517550057 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x65mm 2S Monoaxial
Nuvasive, Inc.
13085065
In Commercial Distribution

  • 00887517550019 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.0x55mm 2S Monoaxial
Nuvasive, Inc.
13085055
In Commercial Distribution

  • 00887517549990 ()


  • 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, 5.0x35mm 2S Monoaxial
Nuvasive, Inc.
13085035
In Commercial Distribution

  • 00887517549952 ()


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