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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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Archon Plate, 36mm 2-Level
Nuvasive, Inc.
8787236
In Commercial Distribution

  • 00887517209306 ()


  • Spinal fixation plate, non-bioabsorbable
ARM15T Rod, 140mm Conventional Pre-Bent
Nuvasive, Inc.
8052140
In Commercial Distribution

  • 00887517209177 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15T Rod, 120mm Conventional Pre-Bent
Nuvasive, Inc.
8052120
In Commercial Distribution

  • 00887517209139 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15T Rod, 110mm Conventional Pre-Bent
Nuvasive, Inc.
8052110
In Commercial Distribution

  • 00887517209115 ()


  • Bone-screw internal spinal fixation system, non-sterile
MAS TLIF Blade, 70mm Lateral Standard
Nuvasive, Inc.
3406070
In Commercial Distribution

  • 00887517209092 ()


  • Surgical retractor/retraction system blade, reusable
MAS TLIF Blade, 60mm Lateral Standard
Nuvasive, Inc.
3406060
In Commercial Distribution

  • 00887517209085 ()


  • Surgical retractor/retraction system blade, reusable
MAS TLIF Blade, 50mm Lateral Standard
Nuvasive, Inc.
3406050
In Commercial Distribution

  • 00887517209078 ()


  • Surgical retractor/retraction system blade, reusable
MAS TLIF Blade, 40mm Lateral Standard
Nuvasive, Inc.
3406040
In Commercial Distribution

  • 00887517209061 ()


  • Surgical retractor/retraction system blade, reusable
MAS TLIF Blade, 110mm Lateral Narrow
Nuvasive, Inc.
3405110
In Commercial Distribution

  • 00887517209054 ()


  • Surgical retractor/retraction system blade, reusable
MAS TLIF Blade, 100mm Lateral Narrow
Nuvasive, Inc.
3405100
In Commercial Distribution

  • 00887517209047 ()


  • Surgical retractor/retraction system blade, reusable
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