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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 Class Implantable

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RELINE-O Screw, 6.5x120mm 2S Reduction
Nuvasive, Inc.
13026512
In Commercial Distribution

  • 00887517540393 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.5x110mm 2S Reduction
Nuvasive, Inc.
13026511
In Commercial Distribution

  • 00887517540386 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.5x100mm 2S Reduction
Nuvasive, Inc.
13026510
In Commercial Distribution

  • 00887517540379 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x95mm 2S Reduction
Nuvasive, Inc.
13026095
In Commercial Distribution

  • 00887517540362 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x90mm 2S Reduction
Nuvasive, Inc.
13026090
In Commercial Distribution

  • 00887517540355 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x85mm 2S Reduction
Nuvasive, Inc.
13026085
In Commercial Distribution

  • 00887517540348 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x80mm 2S Reduction
Nuvasive, Inc.
13026080
In Commercial Distribution

  • 00887517540331 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x75mm 2S Reduction
Nuvasive, Inc.
13026075
In Commercial Distribution

  • 00887517540324 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x70mm 2S Reduction
Nuvasive, Inc.
13026070
In Commercial Distribution

  • 00887517540317 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x65mm 2S Reduction
Nuvasive, Inc.
13026065
In Commercial Distribution

  • 00887517540300 ()


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