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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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CoRoent® XLCT, 10x18x45mm
Nuvasive, Inc.
6101045
In Commercial Distribution

  • 00887517285492 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H Trial, 10mm 30°
Nuvasive, Inc.
6101030
In Commercial Distribution

  • 00887517285485 ()


  • Spinal implant trial
CoRoent XL-H Trial, 10mm 20°
Nuvasive, Inc.
6101020
In Commercial Distribution

  • 00887517285478 ()


  • Spinal implant trial
CoRoent XL-H Trial, 8mm 20°
Nuvasive, Inc.
6100820
In Commercial Distribution

  • 00887517285454 ()


  • Spinal implant trial
CoRoent XL-H Trial, 6mm 20°
Nuvasive, Inc.
6100620
In Commercial Distribution

  • 00887517285430 ()


  • Spinal implant trial
CoRoent XL-H Trial, 4mm 20°
Nuvasive, Inc.
6100420
In Commercial Distribution

  • 00887517285416 ()


  • Spinal implant trial
ARM15S Screw, 10.5x70mm Iliac SL-Closed
Nuvasive, Inc.
8531570
In Commercial Distribution

  • 00887517285386 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 10.5x60mm Iliac SL-Closed
Nuvasive, Inc.
8531560
In Commercial Distribution

  • 00887517285362 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 10.5x120mm Iliac SL-Closed
Nuvasive, Inc.
8531514
In Commercial Distribution

  • 00887517285355 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 10.5x110mm Iliac SL-Closed
Nuvasive, Inc.
8531512
In Commercial Distribution

  • 00887517285331 ()


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