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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 Ant TLIF Ti, 12x10x40mm 12°
Nuvasive, Inc.
5220402P2
In Commercial Distribution

  • 00887517902085 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x36mm 15°
Nuvasive, Inc.
5220365P2
In Commercial Distribution

  • 00887517902078 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x36mm 12°
Nuvasive, Inc.
5220362P2
In Commercial Distribution

  • 00887517902061 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x34mm 8°
Nuvasive, Inc.
5220348P2
In Commercial Distribution

  • 00887517902054 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x34mm 15°
Nuvasive, Inc.
5220345P2
In Commercial Distribution

  • 00887517902047 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x34mm 4°
Nuvasive, Inc.
5220344P2
In Commercial Distribution

  • 00887517902030 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x34mm 12°
Nuvasive, Inc.
5220342P2
In Commercial Distribution

  • 00887517902023 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x34mm 0°
Nuvasive, Inc.
5220340P2
In Commercial Distribution

  • 00887517902016 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x32mm 8°
Nuvasive, Inc.
5220328P2
In Commercial Distribution

  • 00887517902009 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x10x32mm 15°
Nuvasive, Inc.
5220325P2
In Commercial Distribution

  • 00887517901996 ()


  • Metallic spinal interbody fusion cage
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