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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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CoRoent® XLW Ti, 14x22x50mm
Nuvasive, Inc.
6414250
In Commercial Distribution

  • 00887517310521 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 14x22x45mm
Nuvasive, Inc.
6414245
In Commercial Distribution

  • 00887517310514 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x40mm
Nuvasive, Inc.
6414240
In Commercial Distribution

  • 00887517310507 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x60mm
Nuvasive, Inc.
6412260
In Commercial Distribution

  • 00887517310194 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x55mm
Nuvasive, Inc.
6412255
In Commercial Distribution

  • 00887517310187 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x50mm
Nuvasive, Inc.
6412250
In Commercial Distribution

  • 00887517310170 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x45mm
Nuvasive, Inc.
6412245
In Commercial Distribution

  • 00887517310163 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 12x22x40mm
Nuvasive, Inc.
6412240
In Commercial Distribution

  • 00887517310156 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 10x22x60mm
Nuvasive, Inc.
6410260
In Commercial Distribution

  • 00887517310149 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLW Ti, 10x22x55mm
Nuvasive, Inc.
6410255
In Commercial Distribution

  • 00887517310132 ()


  • Polymeric spinal interbody fusion cage
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