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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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Archon Screw, 4.5x17mm S.T. Variable
Nuvasive, Inc.
8881617
In Commercial Distribution

  • 00887517312013 ()


  • Spinal bone screw, non-bioabsorbable
ARM16S Hook, 10mm Lamina Reduced Wide
Nuvasive, Inc.
8563114
In Commercial Distribution

  • 00887517311825 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM16S Hook, 8mm Lamina Reduced Wide
Nuvasive, Inc.
8563113
In Commercial Distribution

  • 00887517311818 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM16S Hook, 6mm Lamina Reduced Wide
Nuvasive, Inc.
8563112
In Commercial Distribution

  • 00887517311801 ()


  • Bone-screw internal spinal fixation system, non-sterile
CoRoent® XL Ti, 8x18x60mm 10°
Nuvasive, Inc.
6480860
In Commercial Distribution

  • 00887517311795 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x55mm 10°
Nuvasive, Inc.
6480855
In Commercial Distribution

  • 00887517311788 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x50mm 10°
Nuvasive, Inc.
6480850
In Commercial Distribution

  • 00887517311771 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x45mm 10°
Nuvasive, Inc.
6480845
In Commercial Distribution

  • 00887517311764 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x40mm 10°
Nuvasive, Inc.
6480840
In Commercial Distribution

  • 00887517311757 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 16x22x60mm 10°
Nuvasive, Inc.
6421660
In Commercial Distribution

  • 00887517311740 ()


  • Polymeric spinal interbody fusion cage
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