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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, 10x18x45mm 10°
Nuvasive, Inc.
6481045
In Commercial Distribution

  • 00887517312112 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x60mm 10°
Nuvasive, Inc.
6480860
In Commercial Distribution

  • 00887517311795 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x55mm 10°
Nuvasive, Inc.
6480855
In Commercial Distribution

  • 00887517311788 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Ti, 8x18x50mm 10°
Nuvasive, Inc.
6480850
In Commercial Distribution

  • 00887517311771 ()


  • 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, 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, 14x22x55mm 10°
Nuvasive, Inc.
6421455
In Commercial Distribution

  • 00887517311382 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x40mm 10°
Nuvasive, Inc.
6421440
In Commercial Distribution

  • 00887517311351 ()


  • Polymeric spinal interbody fusion cage
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