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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 Size Type Device Class Implantable

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Oblique TLIF, 11x10x30mm 12°
Nuvasive, Inc.
5310302P2
In Commercial Distribution

  • 00887517733917 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x30mm 0°
Nuvasive, Inc.
5310300P2
In Commercial Distribution

  • 00887517733900 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x25mm 4°
Nuvasive, Inc.
5310254P2
In Commercial Distribution

  • 00887517733887 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 11x10x25mm 0°
Nuvasive, Inc.
5310250P2
In Commercial Distribution

  • 00887517733863 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x40mm 8°
Nuvasive, Inc.
5304408P2
In Commercial Distribution

  • 00887517733856 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x40mm 4°
Nuvasive, Inc.
5304404P2
In Commercial Distribution

  • 00887517733849 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x40mm 12°
Nuvasive, Inc.
5304402P2
In Commercial Distribution

  • 00887517733832 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x40mm 0°
Nuvasive, Inc.
5304400P2
In Commercial Distribution

  • 00887517733825 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x35mm 8°
Nuvasive, Inc.
5304358P2
In Commercial Distribution

  • 00887517733818 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x35mm 4°
Nuvasive, Inc.
5304354P2
In Commercial Distribution

  • 00887517733801 ()


  • Polymeric spinal interbody fusion cage
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