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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 Screw, 6.0x50mm 2S Reduction
Nuvasive, Inc.
13026050
In Commercial Distribution

  • 00887517540270 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x45mm 2S Reduction
Nuvasive, Inc.
13026045
In Commercial Distribution

  • 00887517540263 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x40mm 2S Reduction
Nuvasive, Inc.
13026040
In Commercial Distribution

  • 00887517540256 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x35mm 2S Reduction
Nuvasive, Inc.
13026035
In Commercial Distribution

  • 00887517540249 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x25mm 2S Reduction
Nuvasive, Inc.
13026025
In Commercial Distribution

  • 00887517540232 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x120mm 2S Reduction
Nuvasive, Inc.
13026012
In Commercial Distribution

  • 00887517540225 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x110mm 2S Reduction
Nuvasive, Inc.
13026011
In Commercial Distribution

  • 00887517540218 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x100mm 2S Reduction
Nuvasive, Inc.
13026010
In Commercial Distribution

  • 00887517540201 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.5x95mm 2S Reduction
Nuvasive, Inc.
13025595
In Commercial Distribution

  • 00887517540195 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.5x90mm 2S Reduction
Nuvasive, Inc.
13025590
In Commercial Distribution

  • 00887517540188 ()


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