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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 LO Titanium, 10x10x30 5°
Nuvasive, Inc.
6081030P
In Commercial Distribution

  • 00887517045713 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 10x10x25 5°
Nuvasive, Inc.
6081025P
In Commercial Distribution

  • 00887517045706 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 9x10x40 5°
Nuvasive, Inc.
6080940P
In Commercial Distribution

  • 00887517032492 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 9x10x35 5°
Nuvasive, Inc.
6080935P
In Commercial Distribution

  • 00887517032485 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 9x10x30 5°
Nuvasive, Inc.
6080930P
In Commercial Distribution

  • 00887517032478 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 14x10x40 5°
Nuvasive, Inc.
6081440P
In Commercial Distribution

  • 00887517046093 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 14x10x35 5°
Nuvasive, Inc.
6081435P
In Commercial Distribution

  • 00887517046086 ()


  • Metallic spinal interbody fusion cage
CoRoent LO, 8x10x35mm 5° Tapered
Nuvasive, Inc.
1625392
In Commercial Distribution

  • 00887517233042 ()


  • Metallic spinal interbody fusion cage
CoRoent LO, 8x10x30mm 5° Tapered
Nuvasive, Inc.
1625391
In Commercial Distribution

  • 00887517233035 ()


  • Metallic spinal interbody fusion cage
CoRoent® LO, 16x10x35mm 5°
Nuvasive, Inc.
6851612
In Commercial Distribution

  • 00887517379566 ()


  • Polymeric spinal interbody fusion cage
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