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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, 14x10x40mm 12°
Nuvasive, Inc.
5340402P2
In Commercial Distribution

  • 00887517735010 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x40mm 0°
Nuvasive, Inc.
5340400P2
In Commercial Distribution

  • 00887517735003 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x35mm 8°
Nuvasive, Inc.
5340358P2
In Commercial Distribution

  • 00887517734990 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x35mm 4°
Nuvasive, Inc.
5340354P2
In Commercial Distribution

  • 00887517734983 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x35mm 12°
Nuvasive, Inc.
5340352P2
In Commercial Distribution

  • 00887517734976 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x35mm 0°
Nuvasive, Inc.
5340350P2
In Commercial Distribution

  • 00887517734969 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x30mm 8°
Nuvasive, Inc.
5340308P2
In Commercial Distribution

  • 00887517734952 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x30mm 4°
Nuvasive, Inc.
5340304P2
In Commercial Distribution

  • 00887517734945 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x30mm 12°
Nuvasive, Inc.
5340302P2
In Commercial Distribution

  • 00887517734938 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 14x10x30mm 0°
Nuvasive, Inc.
5340300P2
In Commercial Distribution

  • 00887517734921 ()


  • Polymeric spinal interbody fusion cage
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