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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, 6.5x45mm Cann
Nuvasive, Inc.
16086545
In Commercial Distribution

  • 00887517559692 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.5x40mm Cann
Nuvasive, Inc.
16086540
In Commercial Distribution

  • 00887517559685 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.5x30mm Cann
Nuvasive, Inc.
16086530
In Commercial Distribution

  • 00887517559661 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.5x110mm Cann
Nuvasive, Inc.
16086511
In Commercial Distribution

  • 00887517559630 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x90mm Cann
Nuvasive, Inc.
16086090
In Commercial Distribution

  • 00887517559609 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x85mm Cann
Nuvasive, Inc.
16086085
In Commercial Distribution

  • 00887517559593 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 6.0x75mm Cann
Nuvasive, Inc.
16086075
In Commercial Distribution

  • 00887517559579 ()


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