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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, 12x18x60mm 10°
Nuvasive, Inc.
6981260P2
In Commercial Distribution

  • 00887517708915 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 12x18x50mm 10°
Nuvasive, Inc.
6981250P2
In Commercial Distribution

  • 00887517708892 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 12x18x40mm 10°
Nuvasive, Inc.
6981240P2
In Commercial Distribution

  • 00887517708878 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 10x18x60mm 10°
Nuvasive, Inc.
6310860P2
In Commercial Distribution

  • 00887517708274 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 10x18x55mm 10°
Nuvasive, Inc.
6310855P2
In Commercial Distribution

  • 00887517708267 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 10x18x50mm 10°
Nuvasive, Inc.
6310850P2
In Commercial Distribution

  • 00887517708250 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 10x18x45mm 10°
Nuvasive, Inc.
6310845P2
In Commercial Distribution

  • 00887517708243 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 10x18x40mm 10°
Nuvasive, Inc.
6310840P2
In Commercial Distribution

  • 00887517708236 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 8x18x60mm 10°
Nuvasive, Inc.
6308860P2
In Commercial Distribution

  • 00887517708175 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 8x18x55mm 10°
Nuvasive, Inc.
6308855P2
In Commercial Distribution

  • 00887517708168 ()


  • Polymeric spinal interbody fusion cage
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