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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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CoRoent LC Ti, 7x11x30mm 8°
Nuvasive, Inc.
6107130
In Commercial Distribution

  • 00887517287335 ()


  • Metallic spinal interbody fusion cage
CoRoent® XLCT, 16x18x60mm
Nuvasive, Inc.
6101660
In Commercial Distribution

  • 00887517287311 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLCT, 16x18x55mm
Nuvasive, Inc.
6101655
In Commercial Distribution

  • 00887517287304 ()


  • Polymeric spinal interbody fusion cage
ARM15S Screw, 9.5x60mm Iliac SL-Closed
Nuvasive, Inc.
8539560
In Commercial Distribution

  • 00887517287281 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 9.5x120mm Iliac SL-Closed
Nuvasive, Inc.
8539514
In Commercial Distribution

  • 00887517287274 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 9.5x110mm Iliac SL-Closed
Nuvasive, Inc.
8539512
In Commercial Distribution

  • 00887517287250 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 9.5x100mm Iliac SL-Closed
Nuvasive, Inc.
8539510
In Commercial Distribution

  • 00887517287236 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 8.5x90mm Iliac SL-Closed
Nuvasive, Inc.
8538590
In Commercial Distribution

  • 00887517287212 ()


  • Bone-screw internal spinal fixation system, non-sterile
CoRoent® XL-CTW, 10x22x55mm, 10°
Nuvasive, Inc.
7221055
In Commercial Distribution

  • 00887517287199 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 10x22x50mm, 10°
Nuvasive, Inc.
7221050
In Commercial Distribution

  • 00887517287182 ()


  • Polymeric spinal interbody fusion cage
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