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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 XL-H Fixation Pin
Nuvasive, Inc.
6200000
In Commercial Distribution

  • 00887517294647 ()


  • Surgical retractor/retraction system blade, reusable
CoRoent XL-FW Drill, Self-Centering
Nuvasive, Inc.
6180015
In Commercial Distribution

  • 00887517293541 ()


  • Cannulated surgical drill bit, reusable
COROENT XL-F WIDE INSTRUMENT TRAY BASE
Nuvasive, Inc.
6180013
In Commercial Distribution

  • 00887517293527 ()


  • Device sterilization/disinfection container, reusable
COROENT XL-F WIDE IMPLANT TRAY BASE
Nuvasive, Inc.
6180004
In Commercial Distribution

  • 00887517293190 ()


  • Device sterilization/disinfection container, reusable
CoRoent® XLFW, 14x22x60mm Lordotic
Nuvasive, Inc.
6171460
In Commercial Distribution

  • 00887517293152 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLFW, 14x22x55mm Lordotic
Nuvasive, Inc.
6171455
In Commercial Distribution

  • 00887517293145 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLFW, 14x22x50mm Lordotic
Nuvasive, Inc.
6171450
In Commercial Distribution

  • 00887517293138 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLFW, 12x22x60mm Lordotic
Nuvasive, Inc.
6171260
In Commercial Distribution

  • 00887517293114 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLFW, 12x22x55mm Lordotic
Nuvasive, Inc.
6171255
In Commercial Distribution

  • 00887517293107 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLFW, 12x22x50mm Lordotic
Nuvasive, Inc.
6171250
In Commercial Distribution

  • 00887517292797 ()


  • Polymeric spinal interbody fusion cage
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