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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, 8x18x60mm 10°
Nuvasive, Inc.
6980860P2
In Commercial Distribution

  • 00887517993946 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 8x18x55mm 10°
Nuvasive, Inc.
6980855P2
In Commercial Distribution

  • 00887517993939 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 8x18x50mm 10°
Nuvasive, Inc.
6980850P2
In Commercial Distribution

  • 00887517993922 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 8x18x45mm 10°
Nuvasive, Inc.
6980845P2
In Commercial Distribution

  • 00887517993915 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 8x18x40mm 10°
Nuvasive, Inc.
6980840P2
In Commercial Distribution

  • 00887517993908 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 12x18x60mm 10°
Nuvasive, Inc.
6312860P2
In Commercial Distribution

  • 00887517993434 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 12x18x55mm 10°
Nuvasive, Inc.
6312855P2
In Commercial Distribution

  • 00887517993427 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 12x18x50mm 10°
Nuvasive, Inc.
6312850P2
In Commercial Distribution

  • 00887517993410 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 12x18x45mm 10°
Nuvasive, Inc.
6312845P2
In Commercial Distribution

  • 00887517993403 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 12x22x60mm 10°
Nuvasive, Inc.
6312260P2
In Commercial Distribution

  • 00887517993397 ()


  • Polymeric spinal interbody fusion cage
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