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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 Class Implantable

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RELINE Screw, 9.5x70mm 2FC Polyaxial
Nuvasive, Inc.
16219570
In Commercial Distribution

  • 00887517924940 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x65mm 2FC Polyaxial
Nuvasive, Inc.
16219565
In Commercial Distribution

  • 00887517924933 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x60mm 2FC Polyaxial
Nuvasive, Inc.
16219560
In Commercial Distribution

  • 00887517924926 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x55mm 2FC Polyaxial
Nuvasive, Inc.
16219555
In Commercial Distribution

  • 00887517924919 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x50mm 2FC Polyaxial
Nuvasive, Inc.
16219550
In Commercial Distribution

  • 00887517924902 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x45mm 2FC Polyaxial
Nuvasive, Inc.
16219545
In Commercial Distribution

  • 00887517924896 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x40mm 2FC Polyaxial
Nuvasive, Inc.
16219540
In Commercial Distribution

  • 00887517924889 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x35mm 2FC Polyaxial
Nuvasive, Inc.
16219535
In Commercial Distribution

  • 00887517924872 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x30mm 2FC Polyaxial
Nuvasive, Inc.
16219530
In Commercial Distribution

  • 00887517924865 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 9.5x100mm 2FC Polyaxial
Nuvasive, Inc.
16219510
In Commercial Distribution

  • 00887517924834 ()


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