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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 Size Type Device Class Implantable

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CoRoent® XL, 12x18x40mm 10°
Nuvasive, Inc.
6981240P
In Commercial Distribution

  • 00887517219879 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 16x18x60mm 10°
Nuvasive, Inc.
6481660P2
In Commercial Distribution

  • 00887517738905 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 16x18x55mm 10°
Nuvasive, Inc.
6481655P2
In Commercial Distribution

  • 00887517738899 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 16x18x50mm 10°
Nuvasive, Inc.
6481650P2
In Commercial Distribution

  • 00887517738882 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 16x18x45mm 10°
Nuvasive, Inc.
6481645P2
In Commercial Distribution

  • 00887517738875 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 16x18x40mm 10°
Nuvasive, Inc.
6481640P2
In Commercial Distribution

  • 00887517738868 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 15x18x60mm 10°
Nuvasive, Inc.
6481560P2
In Commercial Distribution

  • 00887517738851 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 15x18x55mm 10°
Nuvasive, Inc.
6481555P2
In Commercial Distribution

  • 00887517738844 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 15x18x50mm 10°
Nuvasive, Inc.
6481550P2
In Commercial Distribution

  • 00887517738837 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 15x18x45mm 10°
Nuvasive, Inc.
6481545P2
In Commercial Distribution

  • 00887517738820 ()


  • Polymeric spinal interbody fusion cage
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