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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, 8x11x32mm 8°
Nuvasive, Inc.
5281328
In Commercial Distribution

  • 00887517579362 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x11x32mm 4°
Nuvasive, Inc.
5281324
In Commercial Distribution

  • 00887517579355 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x11x32mm 0°
Nuvasive, Inc.
5281320
In Commercial Distribution

  • 00887517579348 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x10x32mm 8°
Nuvasive, Inc.
5280328
In Commercial Distribution

  • 00887517579331 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x10x32mm 4°
Nuvasive, Inc.
5280324
In Commercial Distribution

  • 00887517579324 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x10x32mm 0°
Nuvasive, Inc.
5280320
In Commercial Distribution

  • 00887517579317 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x14x32mm 8°
Nuvasive, Inc.
5264328
In Commercial Distribution

  • 00887517579300 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x14x32mm 4°
Nuvasive, Inc.
5264324
In Commercial Distribution

  • 00887517579294 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x14x32mm 0°
Nuvasive, Inc.
5264320
In Commercial Distribution

  • 00887517579287 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x13x32mm 8°
Nuvasive, Inc.
5263328
In Commercial Distribution

  • 00887517579270 ()


  • Polymeric spinal interbody fusion cage
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