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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 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, 10.5x75mm 2S Reduction
Nuvasive, Inc.
13020575
In Commercial Distribution

  • 00887517538536 ()


  • 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, 10.5x55mm 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
RELINE-O Screw, 10.5x35mm 2S Reduction
Nuvasive, Inc.
13020535
In Commercial Distribution

  • 00887517538451 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x25mm 2S Reduction
Nuvasive, Inc.
13020525
In Commercial Distribution

  • 00887517538437 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.5x100mm 2S Reduction
Nuvasive, Inc.
13020510
In Commercial Distribution

  • 00887517538406 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.5x85mm 2S Poly Iliac
Nuvasive, Inc.
13019585
In Commercial Distribution

  • 00887517538376 ()


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