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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® Large MP, 11x9x28 12°
Nuvasive, Inc.
6121128
In Commercial Distribution

  • 00887517289094 ()


  • Polymeric spinal interbody fusion cage
CoRoent® Large MP, 11x9x23 12°
Nuvasive, Inc.
6121123
In Commercial Distribution

  • 00887517289087 ()


  • Polymeric spinal interbody fusion cage
CoRoent® Large MP, 10x9x28 12°
Nuvasive, Inc.
6121028
In Commercial Distribution

  • 00887517289056 ()


  • Polymeric spinal interbody fusion cage
CoRoent® Large MP, 10x9x23 12°
Nuvasive, Inc.
6121023
In Commercial Distribution

  • 00887517289049 ()


  • Polymeric spinal interbody fusion cage
CoRoent® Large MP, 9x9x28 12°
Nuvasive, Inc.
6120928
In Commercial Distribution

  • 00887517289032 ()


  • Polymeric spinal interbody fusion cage
CoRoent® Large MP, 9x9x23 12°
Nuvasive, Inc.
6120923
In Commercial Distribution

  • 00887517289025 ()


  • Polymeric spinal interbody fusion cage
CoRoent® Large MP, 8x9x28 12°
Nuvasive, Inc.
6120828
In Commercial Distribution

  • 00887517289018 ()


  • Polymeric spinal interbody fusion cage
CoRoent® Large MP, 8x9x23 12°
Nuvasive, Inc.
6120823
In Commercial Distribution

  • 00887517289001 ()


  • Polymeric spinal interbody fusion cage
ARM15S Screw, 8.5x120mm Iliac SL-Open
Nuvasive, Inc.
8548514
In Commercial Distribution

  • 00887517288998 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 8.5x110mm Iliac SL-Open
Nuvasive, Inc.
8548512
In Commercial Distribution

  • 00887517288974 ()


  • Bone-screw internal spinal fixation system, non-sterile
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