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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 Plate, 22mm 1-Level BETA
Nuvasive, Inc.
8888122
In Commercial Distribution

  • 00887517313300 ()


  • Spinal fixation plate, non-bioabsorbable
CoRoent® XL-W+, 8x22x60mm
Nuvasive, Inc.
6508260
In Commercial Distribution

  • 00887517313263 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x55mm
Nuvasive, Inc.
6508255
In Commercial Distribution

  • 00887517313256 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x50mm
Nuvasive, Inc.
6508250
In Commercial Distribution

  • 00887517313249 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x45mm
Nuvasive, Inc.
6508245
In Commercial Distribution

  • 00887517313232 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 8x22x40mm
Nuvasive, Inc.
6508240
In Commercial Distribution

  • 00887517313225 ()


  • Polymeric spinal interbody fusion cage
ARM16S Screw, 5.5x30mm Polyaxial
Nuvasive, Inc.
8565530
In Commercial Distribution

  • 00887517313096 ()


  • Bone-screw internal spinal fixation system, non-sterile
Archon Plate, 21mm 1-Level BETA
Nuvasive, Inc.
8888121
In Commercial Distribution

  • 00887517312990 ()


  • Spinal fixation plate, non-bioabsorbable
Archon Plate, 20mm 1-Level BETA
Nuvasive, Inc.
8888120
In Commercial Distribution

  • 00887517312983 ()


  • Spinal fixation plate, non-bioabsorbable
Archon Plate, 19mm 1-Level BETA
Nuvasive, Inc.
8888119
In Commercial Distribution

  • 00887517312976 ()


  • Spinal fixation plate, non-bioabsorbable
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