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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 Ti, 15x18x40mm 10°
Nuvasive, Inc.
6481540P2
In Commercial Distribution

  • 00887517738813 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 14x18x60mm 10°
Nuvasive, Inc.
6481460P2
In Commercial Distribution

  • 00887517738806 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 14x18x55mm 10°
Nuvasive, Inc.
6481455P2
In Commercial Distribution

  • 00887517738790 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 14x18x50mm 10°
Nuvasive, Inc.
6481450P2
In Commercial Distribution

  • 00887517738783 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 14x18x45mm 10°
Nuvasive, Inc.
6481445P2
In Commercial Distribution

  • 00887517738776 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 14x18x40mm 10°
Nuvasive, Inc.
6481440P2
In Commercial Distribution

  • 00887517738769 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 13x18x60mm 10°
Nuvasive, Inc.
6481360P2
In Commercial Distribution

  • 00887517738752 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 13x18x55mm 10°
Nuvasive, Inc.
6481355P2
In Commercial Distribution

  • 00887517738745 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 13x18x50mm 10°
Nuvasive, Inc.
6481350P2
In Commercial Distribution

  • 00887517738738 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 13x18x45mm 10°
Nuvasive, Inc.
6481345P2
In Commercial Distribution

  • 00887517738721 ()


  • Polymeric spinal interbody fusion cage
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