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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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X-CORE 2 Tamp, Ø16mm Core
Nuvasive, Inc.
6539216
In Commercial Distribution

  • 00887517322005 ()


  • Surgical tamp, reusable
CoRoent XLW Ti, 11x22x50mm 10°
Nuvasive, Inc.
6421150
In Commercial Distribution

  • 00887517321992 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 11x22x45mm 10°
Nuvasive, Inc.
6421145
In Commercial Distribution

  • 00887517321985 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 11x22x40mm 10°
Nuvasive, Inc.
6421140
In Commercial Distribution

  • 00887517321978 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x60mm 10°
Nuvasive, Inc.
6420960
In Commercial Distribution

  • 00887517321961 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x55mm 10°
Nuvasive, Inc.
6420955
In Commercial Distribution

  • 00887517321954 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x50mm 10°
Nuvasive, Inc.
6420950
In Commercial Distribution

  • 00887517321947 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x45mm 10°
Nuvasive, Inc.
6420945
In Commercial Distribution

  • 00887517321930 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x40mm 10°
Nuvasive, Inc.
6420940
In Commercial Distribution

  • 00887517321923 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 15x22x55mm
Nuvasive, Inc.
6415255
In Commercial Distribution

  • 00887517321909 ()


  • Polymeric spinal interbody fusion cage
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