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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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X-CORE 2 Ti Core, Ø22x47-79mm
Nuvasive, Inc.
7220079
In Commercial Distribution

  • 00887517434296 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø22x41-67mm
Nuvasive, Inc.
7220067
In Commercial Distribution

  • 00887517434289 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø22x35-55mm
Nuvasive, Inc.
7220055
In Commercial Distribution

  • 00887517434272 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø22x28-41mm
Nuvasive, Inc.
7220041
In Commercial Distribution

  • 00887517434265 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø22x24-33mm
Nuvasive, Inc.
7220033
In Commercial Distribution

  • 00887517434258 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø22x21-27mm
Nuvasive, Inc.
7220027
In Commercial Distribution

  • 00887517434241 ()


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

  • 00887517434234 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø22x18mm Static
Nuvasive, Inc.
7220018
In Commercial Distribution

  • 00887517434227 ()


  • Vertebral body prosthesis, non-sterile
X-CORE 2 Ti Core, Ø22x16mm Static
Nuvasive, Inc.
7220016
In Commercial Distribution

  • 00887517434210 ()


  • Vertebral body prosthesis, non-sterile
SpheRx® DBR® III Rod, 150mm Pre-Bent
Nuvasive, Inc.
7217150
In Commercial Distribution

  • 00887517433824 ()


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