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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, 9x18x45mm 10°
Nuvasive, Inc.
6480945P2
In Commercial Distribution

  • 00887517738523 ()


  • 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 XLW Ti, 15x22x40mm 10°
Nuvasive, Inc.
6421540P2
In Commercial Distribution

  • 00887517738363 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x60mm 10°
Nuvasive, Inc.
6421460P2
In Commercial Distribution

  • 00887517738356 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x45mm 10°
Nuvasive, Inc.
6421445P2
In Commercial Distribution

  • 00887517738325 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 14x22x40mm 10°
Nuvasive, Inc.
6421440P2
In Commercial Distribution

  • 00887517738318 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 13x22x55mm 10°
Nuvasive, Inc.
6421355P2
In Commercial Distribution

  • 00887517738295 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 13x22x50mm 10°
Nuvasive, Inc.
6421350P2
In Commercial Distribution

  • 00887517738288 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 13x22x45mm 10°
Nuvasive, Inc.
6421345P2
In Commercial Distribution

  • 00887517738271 ()


  • Polymeric spinal interbody fusion cage
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