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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, 8x9x34mm 0°
Nuvasive, Inc.
5289340
In Commercial Distribution

  • 00887517573025 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x32mm 8°
Nuvasive, Inc.
5289328
In Commercial Distribution

  • 00887517573018 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x32mm 4°
Nuvasive, Inc.
5289324
In Commercial Distribution

  • 00887517573001 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x32mm 0°
Nuvasive, Inc.
5289320
In Commercial Distribution

  • 00887517572998 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x30mm 8°
Nuvasive, Inc.
5289308
In Commercial Distribution

  • 00887517572981 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x30mm 4°
Nuvasive, Inc.
5289304
In Commercial Distribution

  • 00887517572974 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x30mm 0°
Nuvasive, Inc.
5289300
In Commercial Distribution

  • 00887517572967 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x28mm 8°
Nuvasive, Inc.
5289288
In Commercial Distribution

  • 00887517572950 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x28mm 4°
Nuvasive, Inc.
5289284
In Commercial Distribution

  • 00887517572943 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x9x28mm 0°
Nuvasive, Inc.
5289280
In Commercial Distribution

  • 00887517572936 ()


  • Polymeric spinal interbody fusion cage
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