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 Size Type Device Class Implantable

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MULTI-AXIAL SCREW DRIVER
Orthofix US LLC
55-1037
In Commercial Distribution

  • 18257200053681 ()


  • Bone-screw internal spinal fixation system, non-sterile
MULTI-AXIAL SCREW DRIVER-NUT
Orthofix US LLC
55-1036
In Commercial Distribution

  • 18257200053674 ()


  • Bone-screw internal spinal fixation system, non-sterile
MONO-AXIAL SCREW DRIVER
Orthofix US LLC
55-1035
In Commercial Distribution

  • 18257200053667 ()


  • Bone-screw internal spinal fixation system, non-sterile
MULTI AXIAL SCREW DRIVER, DISASSEMBLABLE
Orthofix US LLC
52-1931
In Commercial Distribution

  • 18257200047567 ()


  • Bone-screw internal spinal fixation system, non-sterile
MONO AXIAL SCREW DRIVER, DISASSEMBLABLE
Orthofix US LLC
52-1930
In Commercial Distribution

  • 18257200047550 ()


  • Bone-screw internal spinal fixation system, non-sterile
MODULAR SCREW DRIVER, DISASSEMBLABLE
Orthofix US LLC
52-1833
In Commercial Distribution

  • 18257200047529 ()


  • Bone-screw internal spinal fixation system, non-sterile
MODULAR SCREW DRIVER
Orthofix US LLC
52-1832
In Commercial Distribution

  • 18257200047512 ()


  • Bone-screw internal spinal fixation system, non-sterile
MULTI AXIAL SCREW DRIVER
Orthofix US LLC
52-1831
In Commercial Distribution

  • 18257200047505 ()


  • Bone-screw internal spinal fixation system, non-sterile
MONO AXIAL SCREW DRIVER
Orthofix US LLC
52-1830
In Commercial Distribution

  • 18257200047499 ()


  • Bone-screw internal spinal fixation system, non-sterile
MULTI-AXIAL ADJUSTMENT DRIVER
Orthofix US LLC
52-1339
In Commercial Distribution

  • 18257200047376 ()


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