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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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ARM15S Screw, 4x40mm Polyaxial
Nuvasive, Inc.
8554040
In Commercial Distribution

  • 00887517298256 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4x35mm Polyaxial
Nuvasive, Inc.
8554035
In Commercial Distribution

  • 00887517298249 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4x30mm Polyaxial
Nuvasive, Inc.
8554030
In Commercial Distribution

  • 00887517298232 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4x25mm Polyaxial
Nuvasive, Inc.
8554025
In Commercial Distribution

  • 00887517298225 ()


  • Bone-screw internal spinal fixation system, non-sterile
CoRoent® XL-XW, 12x26x50mm
Nuvasive, Inc.
6212050
In Commercial Distribution

  • 00887517298195 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-XW, 12x26x45mm
Nuvasive, Inc.
6212045
In Commercial Distribution

  • 00887517298188 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLK, 18x18x60mm
Nuvasive, Inc.
6211860
In Commercial Distribution

  • 00887517298157 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLK, 18x18x55mm
Nuvasive, Inc.
6211855
In Commercial Distribution

  • 00887517298140 ()


  • Polymeric spinal interbody fusion cage
ARM15T Screw, 5.5x25mm Fixed
Nuvasive, Inc.
8855525
In Commercial Distribution

  • 00887517381217 ()


  • Bone-screw internal spinal fixation system, non-sterile
CoRoent XLF, 20x18x50mm
Nuvasive, Inc.
6862050
In Commercial Distribution

  • 00887517381163 ()


  • Polymeric spinal interbody fusion cage
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