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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, 7.0x60mm 2S Reduction
Nuvasive, Inc.
13027060
In Commercial Distribution

  • 00887517540652 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x55mm 2S Reduction
Nuvasive, Inc.
13027055
In Commercial Distribution

  • 00887517540645 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x50mm 2S Reduction
Nuvasive, Inc.
13027050
In Commercial Distribution

  • 00887517540638 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x45mm 2S Reduction
Nuvasive, Inc.
13027045
In Commercial Distribution

  • 00887517540621 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x40mm 2S Reduction
Nuvasive, Inc.
13027040
In Commercial Distribution

  • 00887517540614 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x35mm 2S Reduction
Nuvasive, Inc.
13027035
In Commercial Distribution

  • 00887517540607 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x30mm 2S Reduction
Nuvasive, Inc.
13027030
In Commercial Distribution

  • 00887517540591 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x25mm 2S Reduction
Nuvasive, Inc.
13027025
In Commercial Distribution

  • 00887517540584 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x120mm 2S Reduction
Nuvasive, Inc.
13027012
In Commercial Distribution

  • 00887517540577 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 7.0x110mm 2S Reduction
Nuvasive, Inc.
13027011
In Commercial Distribution

  • 00887517540560 ()


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