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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, 10.5x65mm Cann
Nuvasive, Inc.
16080565
In Commercial Distribution

  • 00887517557933 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x60mm Cann
Nuvasive, Inc.
16080560
In Commercial Distribution

  • 00887517557926 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x55mm Cann
Nuvasive, Inc.
16080555
In Commercial Distribution

  • 00887517557919 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x50mm Cann
Nuvasive, Inc.
16080550
In Commercial Distribution

  • 00887517557902 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x45mm Cann
Nuvasive, Inc.
16080545
In Commercial Distribution

  • 00887517557896 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x40mm Cann
Nuvasive, Inc.
16080540
In Commercial Distribution

  • 00887517557889 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x35mm Cann
Nuvasive, Inc.
16080535
In Commercial Distribution

  • 00887517557872 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x30mm Cann
Nuvasive, Inc.
16080530
In Commercial Distribution

  • 00887517557865 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x25mm Cann
Nuvasive, Inc.
16080525
In Commercial Distribution

  • 00887517557858 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 10.5x120mm Cann
Nuvasive, Inc.
16080512
In Commercial Distribution

  • 00887517557841 ()


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