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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 XLW Ti, 11x22x40mm 10°
Nuvasive, Inc.
6421140P2
In Commercial Distribution

  • 00887517738165 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 10x22x45mm 10°
Nuvasive, Inc.
6421045P2
In Commercial Distribution

  • 00887517738127 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 10x22x40mm 10°
Nuvasive, Inc.
6421040P2
In Commercial Distribution

  • 00887517738110 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x60mm 10°
Nuvasive, Inc.
6420960P2
In Commercial Distribution

  • 00887517738103 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x55mm 10°
Nuvasive, Inc.
6420955P2
In Commercial Distribution

  • 00887517738097 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x50mm 10°
Nuvasive, Inc.
6420950P2
In Commercial Distribution

  • 00887517738080 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x45mm 10°
Nuvasive, Inc.
6420945P2
In Commercial Distribution

  • 00887517738073 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 9x22x40mm 10°
Nuvasive, Inc.
6420940P2
In Commercial Distribution

  • 00887517738066 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 8x22x55mm 10°
Nuvasive, Inc.
6420855P2
In Commercial Distribution

  • 00887517738042 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 8x22x45mm 10°
Nuvasive, Inc.
6420845P2
In Commercial Distribution

  • 00887517738028 ()


  • Polymeric spinal interbody fusion cage
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