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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 Ant TLIF PEEK, 10x10x34mm 15°
Nuvasive, Inc.
5100345
In Commercial Distribution

  • 00887517635471 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x10x34mm 12°
Nuvasive, Inc.
5100342
In Commercial Distribution

  • 00887517635464 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x10x32mm 15°
Nuvasive, Inc.
5100325
In Commercial Distribution

  • 00887517635457 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x10x32mm 12°
Nuvasive, Inc.
5100322
In Commercial Distribution

  • 00887517635440 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x10x30mm 15°
Nuvasive, Inc.
5100305
In Commercial Distribution

  • 00887517635433 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x10x30mm 12°
Nuvasive, Inc.
5100302
In Commercial Distribution

  • 00887517635426 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x30mm 15°
Nuvasive, Inc.
5299305
In Commercial Distribution

  • 00887517635273 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x30mm 12°
Nuvasive, Inc.
5299302
In Commercial Distribution

  • 00887517635266 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x28mm 15°
Nuvasive, Inc.
5299285
In Commercial Distribution

  • 00887517635259 ()


  • Metallic spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x28mm 12°
Nuvasive, Inc.
5299282
In Commercial Distribution

  • 00887517635242 ()


  • Metallic spinal interbody fusion cage
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