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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 Wide, 8x22x55mm Lordotic
Nuvasive, Inc.
6920855P2
In Commercial Distribution

  • 00887517993847 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Wide, 8x22x50mm Lordotic
Nuvasive, Inc.
6920850P2
In Commercial Distribution

  • 00887517993830 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 10x18x60mm
Nuvasive, Inc.
6910860P2
In Commercial Distribution

  • 00887517993816 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 10x18x45mm
Nuvasive, Inc.
6910845P2
In Commercial Distribution

  • 00887517993786 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Wide, 10x22x60mm
Nuvasive, Inc.
6910260P2
In Commercial Distribution

  • 00887517993762 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Wide, 10x22x55mm
Nuvasive, Inc.
6910255P2
In Commercial Distribution

  • 00887517993755 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL Wide, 10x22x50mm
Nuvasive, Inc.
6910250P2
In Commercial Distribution

  • 00887517993748 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 8x18x60mm
Nuvasive, Inc.
6908860P2
In Commercial Distribution

  • 00887517993724 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 8x18x55mm
Nuvasive, Inc.
6908855P2
In Commercial Distribution

  • 00887517993717 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 8x18x50mm
Nuvasive, Inc.
6908850P2
In Commercial Distribution

  • 00887517993700 ()


  • Polymeric spinal interbody fusion cage
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