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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 Size Type Device Class Implantable

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CoRoent XLR-F, 10x38x28mm 8°
Nuvasive, Inc.
8921038
In Commercial Distribution

  • 00887517390622 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLR-F, 10x34x24mm 8°
Nuvasive, Inc.
8921034
In Commercial Distribution

  • 00887517390615 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 10x22x60mm
Nuvasive, Inc.
6910260
In Commercial Distribution

  • 00887517390547 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 10x22x55mm
Nuvasive, Inc.
6910255
In Commercial Distribution

  • 00887517390530 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 10x22x50mm
Nuvasive, Inc.
6910250
In Commercial Distribution

  • 00887517390523 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 10x22x45mm
Nuvasive, Inc.
6910245
In Commercial Distribution

  • 00887517390516 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 8x18x60mm
Nuvasive, Inc.
6908860
In Commercial Distribution

  • 00887517389725 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 8x18x55mm
Nuvasive, Inc.
6908855
In Commercial Distribution

  • 00887517389718 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 8x18x50mm
Nuvasive, Inc.
6908850
In Commercial Distribution

  • 00887517389701 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL, 8x18x45mm
Nuvasive, Inc.
6908845
In Commercial Distribution

  • 00887517389497 ()


  • Polymeric spinal interbody fusion cage
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