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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 Ant TLIF Ti, 13x12x36mm 4°
Nuvasive, Inc.
5132364
In Commercial Distribution

  • 00887517574770 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x11x40mm 8°
Nuvasive, Inc.
5131408
In Commercial Distribution

  • 00887517574756 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x11x40mm 4°
Nuvasive, Inc.
5131404
In Commercial Distribution

  • 00887517574749 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x11x36mm 8°
Nuvasive, Inc.
5131368
In Commercial Distribution

  • 00887517574725 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x10x40mm 0°
Nuvasive, Inc.
5130400
In Commercial Distribution

  • 00887517574671 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x10x36mm 4°
Nuvasive, Inc.
5130364
In Commercial Distribution

  • 00887517574657 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x9x40mm 8°
Nuvasive, Inc.
5129408
In Commercial Distribution

  • 00887517574633 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x9x36mm 8°
Nuvasive, Inc.
5129368
In Commercial Distribution

  • 00887517574602 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x9x36mm 4°
Nuvasive, Inc.
5129364
In Commercial Distribution

  • 00887517574596 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x9x36mm 0°
Nuvasive, Inc.
5129360
In Commercial Distribution

  • 00887517574589 ()


  • Polymeric spinal interbody fusion cage
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