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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 Class Implantable

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Oblique TLIF, 10x14x35mm 0°
Nuvasive, Inc.
5304350P2
In Commercial Distribution

  • 00887517733788 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x30mm 4°
Nuvasive, Inc.
5304304P2
In Commercial Distribution

  • 00887517733764 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x30mm 0°
Nuvasive, Inc.
5304300P2
In Commercial Distribution

  • 00887517733740 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x25mm 4°
Nuvasive, Inc.
5304254P2
In Commercial Distribution

  • 00887517733726 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x14x25mm 12°
Nuvasive, Inc.
5304252P2
In Commercial Distribution

  • 00887517733719 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x30mm 15°
Nuvasive, Inc.
5303015P2
In Commercial Distribution

  • 00887517733696 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x40mm 8°
Nuvasive, Inc.
5300408P2
In Commercial Distribution

  • 00887517733672 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x40mm 4°
Nuvasive, Inc.
5300404P2
In Commercial Distribution

  • 00887517733665 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x40mm 12°
Nuvasive, Inc.
5300402P2
In Commercial Distribution

  • 00887517733658 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 10x10x40mm 0°
Nuvasive, Inc.
5300400P2
In Commercial Distribution

  • 00887517733641 ()


  • Polymeric spinal interbody fusion cage
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