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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 Class Implantable

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Armada Ti 3CO Impactor, 15mm Cervical
Nuvasive, Inc.
8992502
In Commercial Distribution

  • 00887517235220 ()


  • Orthopaedic implant impactor, reusable
ARM15S Screw, 6.5X45mm PLS
Nuvasive, Inc.
8356545
In Commercial Distribution

  • 00887517235091 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 6.5X35mm PLS
Nuvasive, Inc.
8356535
In Commercial Distribution

  • 00887517235077 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 5.5X55mm PLS
Nuvasive, Inc.
8355555
In Commercial Distribution

  • 00887517235022 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 5.5X50mm PLS
Nuvasive, Inc.
8355550
In Commercial Distribution

  • 00887517235015 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 5.5x45mm PLS
Nuvasive, Inc.
8355545
In Commercial Distribution

  • 00887517235008 ()


  • Bone-screw internal spinal fixation system, non-sterile
Armada Ti 3CO Osteotome, 17mm Lum Ang
Nuvasive, Inc.
8992252
In Commercial Distribution

  • 00887517234889 ()


  • Orthopaedic osteotome
Armada Ti 3CO Osteotome, 12mm Lum
Nuvasive, Inc.
8992241
In Commercial Distribution

  • 00887517234841 ()


  • Orthopaedic osteotome
Armada Ti 3CO Retractor, 12mm Square
Nuvasive, Inc.
8992208
In Commercial Distribution

  • 00887517234827 ()


  • Surgical retraction system, reusable
Armada Ti 3CO Retractor, 10mm Square
Nuvasive, Inc.
8992207
In Commercial Distribution

  • 00887517234810 ()


  • Surgical retraction system, reusable
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