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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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RMM Ti Rod, 4.75x45mm Lordotic Type 2
Nuvasive, Inc.
21547045
In Commercial Distribution

  • 00887517799715 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM Ti Rod, 4.75x40mm Lordotic Type 2
Nuvasive, Inc.
21547040
In Commercial Distribution

  • 00887517799708 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM Ti Rod, 4.75x35mm Lordotic Type 2
Nuvasive, Inc.
21547035
In Commercial Distribution

  • 00887517799692 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM Ti Rod, 4.75x30mm Lordotic Type 2
Nuvasive, Inc.
21547030
In Commercial Distribution

  • 00887517799685 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM Ti Rod, 4.75x25mm Lordotic Type 2
Nuvasive, Inc.
21547025
In Commercial Distribution

  • 00887517799678 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM Ti Rod, 4.75x20mm Lordotic Type 2
Nuvasive, Inc.
21547020
In Commercial Distribution

  • 00887517799661 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM Ti Rod, 4.75x15mm Lordotic Type 2
Nuvasive, Inc.
21547015
In Commercial Distribution

  • 00887517799654 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM CoCr Rod, 4.75x600mm Lordotic
Nuvasive, Inc.
21447600
In Commercial Distribution

  • 00887517799340 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM CoCr Rod, 4.75x500mm Lordotic
Nuvasive, Inc.
21447500
In Commercial Distribution

  • 00887517799333 ()


  • Bone-screw internal spinal fixation system, non-sterile
RMM CoCr Rod, 4.75x400mm Lordotic
Nuvasive, Inc.
21447400
In Commercial Distribution

  • 00887517799326 ()


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