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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 Retractor, 10mm Curved
Nuvasive, Inc.
8992202
In Commercial Distribution

  • 00887517234469 ()


  • Surgical retraction system, reusable
Armada Ti 3CO Retractor, 8mm Curved
Nuvasive, Inc.
8992201
In Commercial Distribution

  • 00887517234452 ()


  • Surgical retraction system, reusable
Armada Ti 3CO Impactor, 40mm Lumbar
Nuvasive, Inc.
8992126
In Commercial Distribution

  • 00887517234445 ()


  • Orthopaedic implant impactor, reusable
Armada Ti 3CO Impactor, 35mm Lumbar
Nuvasive, Inc.
8992125
In Commercial Distribution

  • 00887517234438 ()


  • Orthopaedic implant impactor, reusable
Armada Ti 3CO Impactor, 30mm Lumbar
Nuvasive, Inc.
8992124
In Commercial Distribution

  • 00887517234421 ()


  • Orthopaedic implant impactor, reusable
ARM15S Screw, 4.5X45mm PLS
Nuvasive, Inc.
8354545
In Commercial Distribution

  • 00887517234285 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4.5X40mm PLS
Nuvasive, Inc.
8354540
In Commercial Distribution

  • 00887517234278 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4.5X35mm PLS
Nuvasive, Inc.
8354535
In Commercial Distribution

  • 00887517234261 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4.5X30mm PLS
Nuvasive, Inc.
8354530
In Commercial Distribution

  • 00887517234254 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4.5X25mm PLS
Nuvasive, Inc.
8354525
In Commercial Distribution

  • 00887517234247 ()


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