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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, 10.5x90mm 2S Reduction
Nuvasive, Inc.
13020590
In Commercial Distribution

  • 00887517538567 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x85mm 2S Reduction
Nuvasive, Inc.
13020585
In Commercial Distribution

  • 00887517538550 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x80mm 2S Reduction
Nuvasive, Inc.
13020580
In Commercial Distribution

  • 00887517538543 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x75mm 2S Reduction
Nuvasive, Inc.
13020575
In Commercial Distribution

  • 00887517538536 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x70mm 2S Reduction
Nuvasive, Inc.
13020570
In Commercial Distribution

  • 00887517538529 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x65mm 2S Reduction
Nuvasive, Inc.
13020565
In Commercial Distribution

  • 00887517538512 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x60mm 2S Reduction
Nuvasive, Inc.
13020560
In Commercial Distribution

  • 00887517538505 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x55mm 2S Reduction
Nuvasive, Inc.
13020555
In Commercial Distribution

  • 00887517538499 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x50mm 2S Reduction
Nuvasive, Inc.
13020550
In Commercial Distribution

  • 00887517538482 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x45mm 2S Reduction
Nuvasive, Inc.
13020545
In Commercial Distribution

  • 00887517538475 ()


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