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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 Ant TLIF Ti, 9x14x32mm 8°
Nuvasive, Inc.
5294328
In Commercial Distribution

  • 00887517579607 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x14x32mm 4°
Nuvasive, Inc.
5294324
In Commercial Distribution

  • 00887517579591 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x14x32mm 0°
Nuvasive, Inc.
5294320
In Commercial Distribution

  • 00887517579584 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x13x32mm 8°
Nuvasive, Inc.
5293328
In Commercial Distribution

  • 00887517579577 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x13x32mm 4°
Nuvasive, Inc.
5293324
In Commercial Distribution

  • 00887517579560 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x13x32mm 0°
Nuvasive, Inc.
5293320
In Commercial Distribution

  • 00887517579553 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x12x32mm 8°
Nuvasive, Inc.
5292328
In Commercial Distribution

  • 00887517579546 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x12x32mm 4°
Nuvasive, Inc.
5292324
In Commercial Distribution

  • 00887517579539 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x12x32mm 0°
Nuvasive, Inc.
5292320
In Commercial Distribution

  • 00887517579522 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x11x32mm 8°
Nuvasive, Inc.
5291328
In Commercial Distribution

  • 00887517579515 ()


  • Polymeric spinal interbody fusion cage
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