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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 Size Type Device Class Implantable

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RELINE-O Ti Rod, 5.0x80mm Lordotic
Nuvasive, Inc.
14350080
In Commercial Distribution

  • 00887517507884 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x75mm Lordotic
Nuvasive, Inc.
14350075
In Commercial Distribution

  • 00887517507877 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x70mm Lordotic
Nuvasive, Inc.
14350070
In Commercial Distribution

  • 00887517507860 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x65mm Lordotic
Nuvasive, Inc.
14350065
In Commercial Distribution

  • 00887517507853 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x60mm Lordotic
Nuvasive, Inc.
14350060
In Commercial Distribution

  • 00887517507846 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x55mm Lordotic
Nuvasive, Inc.
14350055
In Commercial Distribution

  • 00887517507839 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x50mm Lordotic
Nuvasive, Inc.
14350050
In Commercial Distribution

  • 00887517507822 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x45mm Lordotic
Nuvasive, Inc.
14350045
In Commercial Distribution

  • 00887517507815 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x40mm Lordotic
Nuvasive, Inc.
14350040
In Commercial Distribution

  • 00887517507808 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x35mm Lordotic
Nuvasive, Inc.
14350035
In Commercial Distribution

  • 00887517507792 ()


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