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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 MAS Trauma Screw, 9.5x90mm Cann
Nuvasive, Inc.
16089590
In Commercial Distribution

  • 00887517560865 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x85mm Cann
Nuvasive, Inc.
16089585
In Commercial Distribution

  • 00887517560858 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x75mm Cann
Nuvasive, Inc.
16089575
In Commercial Distribution

  • 00887517560834 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x70mm Cann
Nuvasive, Inc.
16089570
In Commercial Distribution

  • 00887517560827 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x65mm Cann
Nuvasive, Inc.
16089565
In Commercial Distribution

  • 00887517560810 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x60mm Cann
Nuvasive, Inc.
16089560
In Commercial Distribution

  • 00887517560803 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x40mm Cann
Nuvasive, Inc.
16089540
In Commercial Distribution

  • 00887517560766 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x35mm Cann
Nuvasive, Inc.
16089535
In Commercial Distribution

  • 00887517560759 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x25mm Cann
Nuvasive, Inc.
16089525
In Commercial Distribution

  • 00887517560735 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 9.5x120mm Cann
Nuvasive, Inc.
16089512
In Commercial Distribution

  • 00887517560728 ()


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