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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, 11.5x60mm 2S Reduction
Nuvasive, Inc.
13021560
In Commercial Distribution

  • 00887517539229 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x55mm 2S Reduction
Nuvasive, Inc.
13021555
In Commercial Distribution

  • 00887517539212 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x50mm 2S Reduction
Nuvasive, Inc.
13021550
In Commercial Distribution

  • 00887517539205 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x45mm 2S Reduction
Nuvasive, Inc.
13021545
In Commercial Distribution

  • 00887517539199 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x40mm 2S Reduction
Nuvasive, Inc.
13021540
In Commercial Distribution

  • 00887517539182 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x35mm 2S Reduction
Nuvasive, Inc.
13021535
In Commercial Distribution

  • 00887517539175 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x30mm 2S Reduction
Nuvasive, Inc.
13021530
In Commercial Distribution

  • 00887517539168 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x25mm 2S Reduction
Nuvasive, Inc.
13021525
In Commercial Distribution

  • 00887517539151 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x120mm 2S Reduction
Nuvasive, Inc.
13021512
In Commercial Distribution

  • 00887517539144 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.5x110mm 2S Reduction
Nuvasive, Inc.
13021511
In Commercial Distribution

  • 00887517539137 ()


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