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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 LO Ti, 11x10x40mm 5°
Nuvasive, Inc.
6081140P2
In Commercial Distribution

  • 00887517737113 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 11x10x35mm 5°
Nuvasive, Inc.
6081135P2
In Commercial Distribution

  • 00887517737106 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 11x10x30mm 5°
Nuvasive, Inc.
6081130P2
In Commercial Distribution

  • 00887517737090 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 11x10x25mm 5°
Nuvasive, Inc.
6081125P2
In Commercial Distribution

  • 00887517737083 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 9x10x40mm 5°
Nuvasive, Inc.
6080940P2
In Commercial Distribution

  • 00887517737076 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 9x10x35mm 5°
Nuvasive, Inc.
6080935P2
In Commercial Distribution

  • 00887517737069 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 9x10x30mm 5°
Nuvasive, Inc.
6080930P2
In Commercial Distribution

  • 00887517737052 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Ti, 9x10x25mm 5°
Nuvasive, Inc.
6080925P2
In Commercial Distribution

  • 00887517737045 ()


  • Metallic spinal interbody fusion cage
Oblique TLIF, 9x14x40mm 8°
Nuvasive, Inc.
5394408P2
In Commercial Distribution

  • 00887517737038 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF, 9x14x40mm 4°
Nuvasive, Inc.
5394404P2
In Commercial Distribution

  • 00887517737021 ()


  • Polymeric spinal interbody fusion cage
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