SEARCH RESULTS FOR: gs1(44288 results)

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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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Precept - 00887517393012

PRECEPT Screw, 10.5x25mm Polyaxial TL
Nuvasive, Inc.
8830525A
In Commercial Distribution

  • 00887517393012 ()


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

Precept - 00887517393005

PRECEPT Screw, 10.5x120mm Polyaxial TL
Nuvasive, Inc.
8830520A
In Commercial Distribution

  • 00887517393005 ()


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

CoRoent - 00887517392961

CoRoent® XL, 16x18x60mm
Nuvasive, Inc.
6916860
In Commercial Distribution

  • 00887517392961 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517392954

CoRoent® XL, 16x18x55mm
Nuvasive, Inc.
6916855
In Commercial Distribution

  • 00887517392954 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517392947

CoRoent® XL, 16x18x50mm
Nuvasive, Inc.
6916850
In Commercial Distribution

  • 00887517392947 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517392930

CoRoent® XL, 16x18x45mm
Nuvasive, Inc.
6916845
In Commercial Distribution

  • 00887517392930 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517392923

CoRoent® XL, 16x18x40mm
Nuvasive, Inc.
6916840
In Commercial Distribution

  • 00887517392923 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517392916

CoRoent® XL Wide, 16x22x60mm
Nuvasive, Inc.
6916260
In Commercial Distribution

  • 00887517392916 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517392909

CoRoent® XL Wide, 16x22x55mm
Nuvasive, Inc.
6916255
In Commercial Distribution

  • 00887517392909 ()


  • Polymeric spinal interbody fusion cage

Precept - 00887517392794

PRECEPT Screw, 10.5x110mm Polyaxial TL
Nuvasive, Inc.
8830510A
In Commercial Distribution

  • 00887517392794 ()


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