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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 PEEK, 10x12x32mm 15°
Nuvasive, Inc.
5102325
In Commercial Distribution

  • 00887517635617 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x12x32mm 12°
Nuvasive, Inc.
5102322
In Commercial Distribution

  • 00887517635600 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x12x30mm 15°
Nuvasive, Inc.
5102305
In Commercial Distribution

  • 00887517635594 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x12x30mm 12°
Nuvasive, Inc.
5102302
In Commercial Distribution

  • 00887517635587 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x12x28mm 15°
Nuvasive, Inc.
5102285
In Commercial Distribution

  • 00887517635570 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x12x28mm 12°
Nuvasive, Inc.
5102282
In Commercial Distribution

  • 00887517635563 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x11x34mm 15°
Nuvasive, Inc.
5101345
In Commercial Distribution

  • 00887517635556 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x11x34mm 12°
Nuvasive, Inc.
5101342
In Commercial Distribution

  • 00887517635549 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x11x32mm 15°
Nuvasive, Inc.
5101325
In Commercial Distribution

  • 00887517635532 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 10x11x32mm 12°
Nuvasive, Inc.
5101322
In Commercial Distribution

  • 00887517635525 ()


  • Polymeric spinal interbody fusion cage
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