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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® XL Ti, 8x18x60mm
Nuvasive, Inc.
6808860
In Commercial Distribution

  • 00887517365941 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x55mm
Nuvasive, Inc.
6808855
In Commercial Distribution

  • 00887517365934 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x50mm
Nuvasive, Inc.
6808850
In Commercial Distribution

  • 00887517365927 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x45mm
Nuvasive, Inc.
6808845
In Commercial Distribution

  • 00887517365910 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x40mm
Nuvasive, Inc.
6808840
In Commercial Distribution

  • 00887517365903 ()


  • Polymeric spinal interbody fusion cage
X-CORE 2 Ti Core, Ø22x21-27mm Autolock
Nuvasive, Inc.
7220027A
In Commercial Distribution

  • 00887517365897 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø22x20-25mm Autolock
Nuvasive, Inc.
7220025A
In Commercial Distribution

  • 00887517365880 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø18x68-121mm Autolock
Nuvasive, Inc.
7180121A
In Commercial Distribution

  • 00887517365873 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø18x47-79mm Autolock
Nuvasive, Inc.
7180079A
In Commercial Distribution

  • 00887517365866 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø18x41-67mm Autolock
Nuvasive, Inc.
7180067A
In Commercial Distribution

  • 00887517365859 ()


  • Vertebral body prosthesis, non-sterile
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