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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CoRoent - 00887517368119

CoRoent® XL Ti, 12x18x40mm
Nuvasive, Inc.
6812840
In Commercial Distribution

  • 00887517368119 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517368102

CoRoent® Small, 12x13x15mm Lordotic Plus
Nuvasive, Inc.
6812815
In Commercial Distribution

  • 00887517368102 ()


  • Polymeric spinal interbody fusion cage

Precept - 00887517368027

PRECEPT Reduction Screw, 8.5x60mm
Nuvasive, Inc.
8828560
In Commercial Distribution

  • 00887517368027 ()


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

Precept - 00887517368010

PRECEPT Reduction Screw, 8.5x55mm
Nuvasive, Inc.
8828555
In Commercial Distribution

  • 00887517368010 ()


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

Precept - 00887517368003

PRECEPT Reduction Screw, 8.5x50mm
Nuvasive, Inc.
8828550
In Commercial Distribution

  • 00887517368003 ()


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

CoRoent - 00887517367990

Oblique TLIF Trial, 10x14x30mm 5°
Nuvasive, Inc.
1657643
In Commercial Distribution

  • 00887517367990 ()


  • Spinal implant trial

CoRoent - 00887517367976

Oblique TLIF Trial, 8x14x30mm 5°
Nuvasive, Inc.
1657641
In Commercial Distribution

  • 00887517367976 ()


  • Spinal implant trial

CoRoent - 00887517367792

CoRoent® Small, 12x11x14mm 5° Lordotic
Nuvasive, Inc.
6812714
In Commercial Distribution

  • 00887517367792 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517367785

CoRoent® XLW, 12x22x40mm Lordotic
Nuvasive, Inc.
6812340
In Commercial Distribution

  • 00887517367785 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517367778

CoRoent® XLW, 12x22x40mm
Nuvasive, Inc.
6812240
In Commercial Distribution

  • 00887517367778 ()


  • Polymeric spinal interbody fusion cage
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