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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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SpheRx® EXT Rod, 95mm Pre-Bent
Nuvasive, Inc.
7783095
In Commercial Distribution

  • 00887517125583 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 90mm Pre-Bent
Nuvasive, Inc.
7783090
In Commercial Distribution

  • 00887517125576 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 85mm Pre-Bent
Nuvasive, Inc.
7783085
In Commercial Distribution

  • 00887517125569 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 80mm Pre-Bent
Nuvasive, Inc.
7783080
In Commercial Distribution

  • 00887517125552 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 75mm Pre-Bent
Nuvasive, Inc.
7783075
In Commercial Distribution

  • 00887517125545 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 70mm Pre-Bent
Nuvasive, Inc.
7783070
In Commercial Distribution

  • 00887517125538 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 65mm Pre-Bent
Nuvasive, Inc.
7783065
In Commercial Distribution

  • 00887517125521 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 60mm Pre-Bent
Nuvasive, Inc.
7783060
In Commercial Distribution

  • 00887517125514 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 55mm Pre-Bent
Nuvasive, Inc.
7783055
In Commercial Distribution

  • 00887517125507 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® EXT Rod, 50mm Pre-Bent
Nuvasive, Inc.
7783050
In Commercial Distribution

  • 00887517125095 ()


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