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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, 13x9x30mm 8°
Nuvasive, Inc.
5239308
In Commercial Distribution

  • 00887517570703 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x9x30mm 4°
Nuvasive, Inc.
5239304
In Commercial Distribution

  • 00887517570697 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x9x30mm 0°
Nuvasive, Inc.
5239300
In Commercial Distribution

  • 00887517570680 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x9x28mm 8°
Nuvasive, Inc.
5239288
In Commercial Distribution

  • 00887517570673 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x9x28mm 4°
Nuvasive, Inc.
5239284
In Commercial Distribution

  • 00887517570666 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x9x28mm 0°
Nuvasive, Inc.
5239280
In Commercial Distribution

  • 00887517570659 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x14x34mm 8°
Nuvasive, Inc.
5234348
In Commercial Distribution

  • 00887517570642 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x14x34mm 4°
Nuvasive, Inc.
5234344
In Commercial Distribution

  • 00887517570635 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x14x34mm 0°
Nuvasive, Inc.
5234340
In Commercial Distribution

  • 00887517570628 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 13x14x30mm 8°
Nuvasive, Inc.
5234308
In Commercial Distribution

  • 00887517570611 ()


  • Polymeric spinal interbody fusion cage
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