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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 Class Implantable

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CoRoent LO, 10x10x35mm 10°
Nuvasive, Inc.
1552256P2
In Commercial Distribution

  • 00887517732781 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 8x10x35mm 10°
Nuvasive, Inc.
1552255P2
In Commercial Distribution

  • 00887517732774 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 12x10x30mm 10°
Nuvasive, Inc.
1552253P2
In Commercial Distribution

  • 00887517732767 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 10x10x30mm 10°
Nuvasive, Inc.
1552252P2
In Commercial Distribution

  • 00887517732750 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 8x10x30mm 10°
Nuvasive, Inc.
1552251P2
In Commercial Distribution

  • 00887517732743 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x65mm 15°
Nuvasive, Inc.
7161665
In Commercial Distribution

  • 00887517731807 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x60mm 15°
Nuvasive, Inc.
7161660
In Commercial Distribution

  • 00887517731784 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x55mm 15°
Nuvasive, Inc.
7161655
In Commercial Distribution

  • 00887517731760 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x50mm 15°
Nuvasive, Inc.
7161650
In Commercial Distribution

  • 00887517731746 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x45mm 15°
Nuvasive, Inc.
7161645
In Commercial Distribution

  • 00887517731722 ()


  • Polymeric spinal interbody fusion cage
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