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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RELINE-C Ti Rod, Ø3.5-Ø5.5 200/500mm T
Nuvasive, Inc.
3749109
In Commercial Distribution

  • 00887517005113 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, Ø3.5-Ø5.0 200/500mm T
Nuvasive, Inc.
3749108
In Commercial Distribution

  • 00887517005106 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, Ø3.5-Ø4.5 200/500mm T
Nuvasive, Inc.
3749107
In Commercial Distribution

  • 00887517005090 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, Ø3.5-Ø4.0 200/500mm T
Nuvasive, Inc.
3749106
In Commercial Distribution

  • 00887517005083 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, Ø3.5-Ø6.0 220/265mm T
Nuvasive, Inc.
3749105
In Commercial Distribution

  • 00887517005076 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, Ø3.5-Ø5.5 220/265mm T
Nuvasive, Inc.
3749104
In Commercial Distribution

  • 00887517005069 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, Ø3.5-Ø5.0 220/265mm T
Nuvasive, Inc.
3749103
In Commercial Distribution

  • 00887517005052 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, Ø3.5-Ø4.5 220/265mm T
Nuvasive, Inc.
3749102
In Commercial Distribution

  • 00887517005045 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, Ø3.5-Ø4.0 220/265mm T
Nuvasive, Inc.
3749101
In Commercial Distribution

  • 00887517005038 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C CoCr Rod, 4.0x120mm Pre-Bent
Nuvasive, Inc.
3748120
In Commercial Distribution

  • 00887517005021 ()


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