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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, 12.5x95mm 2S Reduction
Nuvasive, Inc.
13022595
In Commercial Distribution

  • 00887517539472 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x90mm 2S Reduction
Nuvasive, Inc.
13022590
In Commercial Distribution

  • 00887517539465 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x85mm 2S Reduction
Nuvasive, Inc.
13022585
In Commercial Distribution

  • 00887517539458 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x80mm 2S Reduction
Nuvasive, Inc.
13022580
In Commercial Distribution

  • 00887517539441 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x75mm 2S Reduction
Nuvasive, Inc.
13022575
In Commercial Distribution

  • 00887517539434 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x70mm 2S Reduction
Nuvasive, Inc.
13022570
In Commercial Distribution

  • 00887517539427 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x65mm 2S Reduction
Nuvasive, Inc.
13022565
In Commercial Distribution

  • 00887517539410 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x60mm 2S Reduction
Nuvasive, Inc.
13022560
In Commercial Distribution

  • 00887517539403 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x55mm 2S Reduction
Nuvasive, Inc.
13022555
In Commercial Distribution

  • 00887517539397 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x50mm 2S Reduction
Nuvasive, Inc.
13022550
In Commercial Distribution

  • 00887517539380 ()


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