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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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RELINE C Ti Rod, 4.0x25mm Pre Bent
Nuvasive, Inc.
3944025
In Commercial Distribution

  • 00195377072986 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x120mm Pre Bent
Nuvasive, Inc.
3943120
In Commercial Distribution

  • 00195377072962 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x110mm Pre Bent
Nuvasive, Inc.
3943110
In Commercial Distribution

  • 00195377072948 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x100mm Pre Bent
Nuvasive, Inc.
3943100
In Commercial Distribution

  • 00195377072924 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x90mm Pre Bent
Nuvasive, Inc.
3943090
In Commercial Distribution

  • 00195377072900 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x80mm Pre Bent
Nuvasive, Inc.
3943080
In Commercial Distribution

  • 00195377072887 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x70mm Pre Bent
Nuvasive, Inc.
3943070
In Commercial Distribution

  • 00195377072863 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x60mm Pre Bent
Nuvasive, Inc.
3943060
In Commercial Distribution

  • 00195377072849 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x50mm Pre Bent
Nuvasive, Inc.
3943050
In Commercial Distribution

  • 00195377072825 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Ti Rod, 3.5x40mm Pre Bent
Nuvasive, Inc.
3943040
In Commercial Distribution

  • 00195377072801 ()


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