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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, 8x11x30mm 0°
Nuvasive, Inc.
5281300
In Commercial Distribution

  • 00887517572608 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x11x28mm 8°
Nuvasive, Inc.
5281288
In Commercial Distribution

  • 00887517572592 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x10x34mm 8°
Nuvasive, Inc.
5280348
In Commercial Distribution

  • 00887517572561 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x10x34mm 4°
Nuvasive, Inc.
5280344
In Commercial Distribution

  • 00887517572554 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x10x34mm 0°
Nuvasive, Inc.
5280340
In Commercial Distribution

  • 00887517572547 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x10x30mm 4°
Nuvasive, Inc.
5280304
In Commercial Distribution

  • 00887517572523 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x10x28mm 4°
Nuvasive, Inc.
5280284
In Commercial Distribution

  • 00887517572493 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x9x34mm 8°
Nuvasive, Inc.
5269348
In Commercial Distribution

  • 00887517572479 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x9x34mm 4°
Nuvasive, Inc.
5269344
In Commercial Distribution

  • 00887517572462 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x9x32mm 0°
Nuvasive, Inc.
5269320
In Commercial Distribution

  • 00887517572424 ()


  • Polymeric spinal interbody fusion cage
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