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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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Interlock HL Guide, Adjustable Drill
Nuvasive, Inc.
1568640
In Commercial Distribution

  • 00887517723598 ()


  • Surgical instrument/implant depth limiter
CoRoent LI, 16x9x26mm 4°
Nuvasive, Inc.
6716926P2
In Commercial Distribution

  • 00887517723550 ()


  • Polymeric spinal interbody fusion cage
CoRoent LI, 16x9x20mm 4°
Nuvasive, Inc.
6716920P2
In Commercial Distribution

  • 00887517723543 ()


  • Polymeric spinal interbody fusion cage
CoRoent LI, 15x9x32mm 4°
Nuvasive, Inc.
6715932P2
In Commercial Distribution

  • 00887517723536 ()


  • Polymeric spinal interbody fusion cage
CoRoent LI, 15x9x26mm 4°
Nuvasive, Inc.
6715926P2
In Commercial Distribution

  • 00887517723529 ()


  • Polymeric spinal interbody fusion cage
CoRoent LI, 15x9x20mm 4°
Nuvasive, Inc.
6715920P2
In Commercial Distribution

  • 00887517723512 ()


  • Polymeric spinal interbody fusion cage
CoRoent LI, 14x9x26mm 4°
Nuvasive, Inc.
6714926P2
In Commercial Distribution

  • 00887517723499 ()


  • Polymeric spinal interbody fusion cage
CoRoent LT, 14x9x25mm 8°
Nuvasive, Inc.
6714825P2
In Commercial Distribution

  • 00887517723475 ()


  • Polymeric spinal interbody fusion cage
CoRoent LT, 14x9x25mm 15°
Nuvasive, Inc.
6714525P2
In Commercial Distribution

  • 00887517723451 ()


  • Polymeric spinal interbody fusion cage
CoRoent LT, 14x9x20mm 15°
Nuvasive, Inc.
6714520P2
In Commercial Distribution

  • 00887517723444 ()


  • Polymeric spinal interbody fusion cage
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