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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, 10x9x40mm 8°
Nuvasive, Inc.
5109408
In Commercial Distribution

  • 00887517573971 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x40mm 4°
Nuvasive, Inc.
5109404
In Commercial Distribution

  • 00887517573964 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x40mm 0°
Nuvasive, Inc.
5109400
In Commercial Distribution

  • 00887517573957 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x36mm 8°
Nuvasive, Inc.
5109368
In Commercial Distribution

  • 00887517573940 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x36mm 4°
Nuvasive, Inc.
5109364
In Commercial Distribution

  • 00887517573933 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x36mm 0°
Nuvasive, Inc.
5109360
In Commercial Distribution

  • 00887517573926 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x14x40mm 8°
Nuvasive, Inc.
5104408
In Commercial Distribution

  • 00887517573919 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x14x40mm 4°
Nuvasive, Inc.
5104404
In Commercial Distribution

  • 00887517573902 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x14x40mm 0°
Nuvasive, Inc.
5104400
In Commercial Distribution

  • 00887517573896 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x14x36mm 8°
Nuvasive, Inc.
5104368
In Commercial Distribution

  • 00887517573889 ()


  • Polymeric spinal interbody fusion cage
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