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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, 10x18x40mm 10°
Nuvasive, Inc.
6481040P2
In Commercial Distribution

  • 00887517738561 ()


  • Metallic spinal interbody fusion cage
CoRoent XL Ti, 9x18x55mm 10°
Nuvasive, Inc.
6480955P2
In Commercial Distribution

  • 00887517738547 ()


  • Metallic spinal interbody fusion cage
CoRoent XL Ti, 8x18x55mm 10°
Nuvasive, Inc.
6480855P2
In Commercial Distribution

  • 00887517738493 ()


  • Metallic spinal interbody fusion cage
CoRoent XL Ti, 8x18x40mm 10°
Nuvasive, Inc.
6480840P2
In Commercial Distribution

  • 00887517738462 ()


  • Metallic spinal interbody fusion cage
CoRoent XLW Ti, 16x22x60mm 10°
Nuvasive, Inc.
6421660P2
In Commercial Distribution

  • 00887517738455 ()


  • Metallic spinal interbody fusion cage
CoRoent XLW Ti, 16x22x55mm 10°
Nuvasive, Inc.
6421655P2
In Commercial Distribution

  • 00887517738448 ()


  • Metallic spinal interbody fusion cage
CoRoent XLW Ti, 16x22x50mm 10°
Nuvasive, Inc.
6421650P2
In Commercial Distribution

  • 00887517738431 ()


  • Metallic spinal interbody fusion cage
CoRoent XLW Ti, 16x22x45mm 10°
Nuvasive, Inc.
6421645P2
In Commercial Distribution

  • 00887517738424 ()


  • Metallic spinal interbody fusion cage
CoRoent XLW Ti, 16x22x40mm 10°
Nuvasive, Inc.
6421640P2
In Commercial Distribution

  • 00887517738417 ()


  • Metallic spinal interbody fusion cage
CoRoent XLW Ti, 15x22x60mm 10°
Nuvasive, Inc.
6421560P2
In Commercial Distribution

  • 00887517738400 ()


  • Metallic spinal interbody fusion cage
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