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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, 9x14x28mm 15°
Nuvasive, Inc.
5194285
In Commercial Distribution

  • 00887517639578 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x14x28mm 12°
Nuvasive, Inc.
5194282
In Commercial Distribution

  • 00887517639561 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x13x34mm 15°
Nuvasive, Inc.
5193345
In Commercial Distribution

  • 00887517639554 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x13x34mm 12°
Nuvasive, Inc.
5193342
In Commercial Distribution

  • 00887517639547 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x13x32mm 15°
Nuvasive, Inc.
5193325
In Commercial Distribution

  • 00887517639530 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x13x32mm 12°
Nuvasive, Inc.
5193322
In Commercial Distribution

  • 00887517639523 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x13x30mm 15°
Nuvasive, Inc.
5193305
In Commercial Distribution

  • 00887517639516 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x13x30mm 12°
Nuvasive, Inc.
5193302
In Commercial Distribution

  • 00887517639509 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x13x28mm 15°
Nuvasive, Inc.
5193285
In Commercial Distribution

  • 00887517639493 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 9x13x28mm 12°
Nuvasive, Inc.
5193282
In Commercial Distribution

  • 00887517639486 ()


  • Polymeric spinal interbody fusion cage
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