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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, 8x9x25 8°
Nuvasive, Inc.
6608925P2
In Commercial Distribution

  • 00887517682710 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-L+, 8x16x45mm 10°
Nuvasive, Inc.
6308645006P2
In Commercial Distribution

  • 00887517681607 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 10x22x60mm 30°
Nuvasive, Inc.
6301060P2
In Commercial Distribution

  • 00887517681539 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 10x22x40mm 30°
Nuvasive, Inc.
6301040P2
In Commercial Distribution

  • 00887517681492 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 8x22x60mm 30°
Nuvasive, Inc.
6300860P2
In Commercial Distribution

  • 00887517681485 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 8x22x40mm 30°
Nuvasive, Inc.
6300840P2
In Commercial Distribution

  • 00887517681447 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 6x22x60mm 30°
Nuvasive, Inc.
6300660P2
In Commercial Distribution

  • 00887517681430 ()


  • Spinal implant trial
CoRoent XL-H, 6x22x40mm 30°
Nuvasive, Inc.
6300640P2
In Commercial Distribution

  • 00887517681393 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 4x22x60mm 30°
Nuvasive, Inc.
6300460P2
In Commercial Distribution

  • 00887517681386 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 4x22x40mm 30°
Nuvasive, Inc.
6300440P2
In Commercial Distribution

  • 00887517681348 ()


  • Polymeric spinal interbody fusion cage
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