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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, 12x11x28mm 0°
Nuvasive, Inc.
5221280
In Commercial Distribution

  • 00887517569721 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x34mm 8°
Nuvasive, Inc.
5220348
In Commercial Distribution

  • 00887517569714 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x34mm 4°
Nuvasive, Inc.
5220344
In Commercial Distribution

  • 00887517569707 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x34mm 0°
Nuvasive, Inc.
5220340
In Commercial Distribution

  • 00887517569691 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x30mm 8°
Nuvasive, Inc.
5220308
In Commercial Distribution

  • 00887517569684 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x30mm 4°
Nuvasive, Inc.
5220304
In Commercial Distribution

  • 00887517569677 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x30mm 0°
Nuvasive, Inc.
5220300
In Commercial Distribution

  • 00887517569660 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x28mm 8°
Nuvasive, Inc.
5220288
In Commercial Distribution

  • 00887517569653 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x28mm 4°
Nuvasive, Inc.
5220284
In Commercial Distribution

  • 00887517569646 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x28mm 0°
Nuvasive, Inc.
5220280
In Commercial Distribution

  • 00887517569639 ()


  • Polymeric spinal interbody fusion cage
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