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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, 11x22x55mm 10°
Nuvasive, Inc.
6421155P2
In Commercial Distribution

  • 00887517738196 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLW Ti, 11x22x50mm 10°
Nuvasive, Inc.
6421150P2
In Commercial Distribution

  • 00887517738189 ()


  • 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, 9x22x50mm 10°
Nuvasive, Inc.
6420950P2
In Commercial Distribution

  • 00887517738080 ()


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

  • 00887517738066 ()


  • Polymeric spinal interbody fusion cage
BASE Ti 10° Implants Set
Nuvasive, Inc.
BASEIMP10
In Commercial Distribution

  • 00887517725271 ()


  • Device sterilization/disinfection container, reusable
BASE Ti Implant, 8x42x30mm 10°
Nuvasive, Inc.
6953810
In Commercial Distribution

  • 00887517701336 ()


  • Metallic spinal interbody fusion cage
BASE Ti Implant, 6x42x30mm 10°
Nuvasive, Inc.
6953610
In Commercial Distribution

  • 00887517701282 ()


  • Metallic spinal interbody fusion cage
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