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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® XL Ti, 8x18x45mm 10°
Nuvasive, Inc.
6480845
In Commercial Distribution

  • 00887517311764 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x40mm 10°
Nuvasive, Inc.
6480840
In Commercial Distribution

  • 00887517311757 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 16x22x60mm 10°
Nuvasive, Inc.
6421660
In Commercial Distribution

  • 00887517311740 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 16x22x55mm 10°
Nuvasive, Inc.
6421655
In Commercial Distribution

  • 00887517311733 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 16x22x50mm 10°
Nuvasive, Inc.
6421650
In Commercial Distribution

  • 00887517311726 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 16x22x45mm 10°
Nuvasive, Inc.
6421645
In Commercial Distribution

  • 00887517311719 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 16x22x40mm 10°
Nuvasive, Inc.
6421640
In Commercial Distribution

  • 00887517311702 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x60mm 10°
Nuvasive, Inc.
6421460
In Commercial Distribution

  • 00887517311399 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x55mm 10°
Nuvasive, Inc.
6421455
In Commercial Distribution

  • 00887517311382 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x50mm 10°
Nuvasive, Inc.
6421450
In Commercial Distribution

  • 00887517311375 ()


  • Polymeric spinal interbody fusion cage
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