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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, 9x18x55mm 10°
Nuvasive, Inc.
6480955P2
In Commercial Distribution

  • 00887517738547 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 9x18x50mm 10°
Nuvasive, Inc.
6480950P2
In Commercial Distribution

  • 00887517738530 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 9x18x45mm 10°
Nuvasive, Inc.
6480945P2
In Commercial Distribution

  • 00887517738523 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 9x18x40mm 10°
Nuvasive, Inc.
6480940P2
In Commercial Distribution

  • 00887517738516 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Ti, 8x18x60mm 10°
Nuvasive, Inc.
6480860P2
In Commercial Distribution

  • 00887517738509 ()


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

  • 00887517738493 ()


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

  • 00887517738462 ()


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

  • 00887517738455 ()


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

  • 00887517738448 ()


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

  • 00887517738431 ()


  • Polymeric spinal interbody fusion cage
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