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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 MAS Trauma Screw, 6.0x70mm Cann
Nuvasive, Inc.
16086070
In Commercial Distribution

  • 00887517559562 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x65mm Cann
Nuvasive, Inc.
16086065
In Commercial Distribution

  • 00887517559555 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x60mm Cann
Nuvasive, Inc.
16086060
In Commercial Distribution

  • 00887517559548 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x55mm Cann
Nuvasive, Inc.
16086055
In Commercial Distribution

  • 00887517559531 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x50mm Cann
Nuvasive, Inc.
16086050
In Commercial Distribution

  • 00887517559524 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x35mm Cann
Nuvasive, Inc.
16086035
In Commercial Distribution

  • 00887517559494 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x25mm Cann
Nuvasive, Inc.
16086025
In Commercial Distribution

  • 00887517559470 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x120mm Cann
Nuvasive, Inc.
16086012
In Commercial Distribution

  • 00887517559463 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x100mm Cann
Nuvasive, Inc.
16086010
In Commercial Distribution

  • 00887517559449 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 5.5x95mm Cann
Nuvasive, Inc.
16085595
In Commercial Distribution

  • 00887517559432 ()


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