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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, 9.0x25mm 2S Polyaxial
Nuvasive, Inc.
13019025
In Commercial Distribution

  • 00887517538079 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x100mm 2S Poly Iliac
Nuvasive, Inc.
13019010
In Commercial Distribution

  • 00887517538048 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x90mm 2S Poly Iliac
Nuvasive, Inc.
13018590
In Commercial Distribution

  • 00887517538024 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x80mm 2S Poly Iliac
Nuvasive, Inc.
13018580
In Commercial Distribution

  • 00887517538000 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x75mm 2S Poly Iliac
Nuvasive, Inc.
13018575
In Commercial Distribution

  • 00887517537997 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x70mm 2S Poly Iliac
Nuvasive, Inc.
13018570
In Commercial Distribution

  • 00887517537980 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x65mm 2S Poly Iliac
Nuvasive, Inc.
13018565
In Commercial Distribution

  • 00887517537973 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x60mm 2S Poly Iliac
Nuvasive, Inc.
13018560
In Commercial Distribution

  • 00887517537966 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x55mm 2S Polyaxial
Nuvasive, Inc.
13018555
In Commercial Distribution

  • 00887517537959 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x50mm 2S Polyaxial
Nuvasive, Inc.
13018550
In Commercial Distribution

  • 00887517537942 ()


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