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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 Osteotome, 7mm Lum Ang
Nuvasive, Inc.
8992250
In Commercial Distribution

  • 00887517234865 ()


  • 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
Armada Ti 3CO Retractor, 8mm Square
Nuvasive, Inc.
8992206
In Commercial Distribution

  • 00887517234803 ()


  • Surgical retraction system, reusable
ARM15S Screw, 5.5X40mm PLS
Nuvasive, Inc.
8355540
In Commercial Distribution

  • 00887517234698 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 5.5X35mm PLS
Nuvasive, Inc.
8355535
In Commercial Distribution

  • 00887517234681 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 5.5X25mm PLS
Nuvasive, Inc.
8355525
In Commercial Distribution

  • 00887517234667 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 5X50mm PLS
Nuvasive, Inc.
8355050
In Commercial Distribution

  • 00887517234650 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 5x40mm PLS
Nuvasive, Inc.
8355040
In Commercial Distribution

  • 00887517234636 ()


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