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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, 10x10x30mm 5°
Nuvasive, Inc.
6851011P2
In Commercial Distribution

  • 00887517683830 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 10x10x25mm 5°
Nuvasive, Inc.
6851010P2
In Commercial Distribution

  • 00887517683816 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 8x10x35mm 5°
Nuvasive, Inc.
6850812P2
In Commercial Distribution

  • 00887517683731 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 8x10x30mm 5°
Nuvasive, Inc.
6850811P2
In Commercial Distribution

  • 00887517683717 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO, 8x10x25mm 5°
Nuvasive, Inc.
6850810P2
In Commercial Distribution

  • 00887517683694 ()


  • Polymeric spinal interbody fusion cage
CoRoent LC, 14x9x25 8°
Nuvasive, Inc.
6614925P2
In Commercial Distribution

  • 00887517682956 ()


  • Polymeric spinal interbody fusion cage
CoRoent LC, 12x9x25 8°
Nuvasive, Inc.
6612925P2
In Commercial Distribution

  • 00887517682871 ()


  • Polymeric spinal interbody fusion cage
CoRoent LC, 10x9x25 8°
Nuvasive, Inc.
6610925P2
In Commercial Distribution

  • 00887517682796 ()


  • Polymeric spinal interbody fusion cage
CoRoent LC, 8x9x25 8°
Nuvasive, Inc.
6608925P2
In Commercial Distribution

  • 00887517682710 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 16x9x28mm 12°
Nuvasive, Inc.
6121628P2
In Commercial Distribution

  • 00887517680303 ()


  • Polymeric spinal interbody fusion cage
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