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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, 9.5x70mm 2S Monoaxial
Nuvasive, Inc.
13089570
In Commercial Distribution

  • 00887517551641 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x65mm 2S Monoaxial
Nuvasive, Inc.
13089565
In Commercial Distribution

  • 00887517551634 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x60mm 2S Monoaxial
Nuvasive, Inc.
13089560
In Commercial Distribution

  • 00887517551627 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x55mm 2S Monoaxial
Nuvasive, Inc.
13089555
In Commercial Distribution

  • 00887517551610 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x50mm 2S Monoaxial
Nuvasive, Inc.
13089550
In Commercial Distribution

  • 00887517551603 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x45mm 2S Monoaxial
Nuvasive, Inc.
13089545
In Commercial Distribution

  • 00887517551597 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x40mm 2S Monoaxial
Nuvasive, Inc.
13089540
In Commercial Distribution

  • 00887517551580 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x35mm 2S Monoaxial
Nuvasive, Inc.
13089535
In Commercial Distribution

  • 00887517551573 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x30mm 2S Monoaxial
Nuvasive, Inc.
13089530
In Commercial Distribution

  • 00887517551566 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x25mm 2S Monoaxial
Nuvasive, Inc.
13089525
In Commercial Distribution

  • 00887517551559 ()


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