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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+, 12x18x60mm
Nuvasive, Inc.
6012860P2
In Commercial Distribution

  • 00887517992994 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 12x18x45mm
Nuvasive, Inc.
6012845P2
In Commercial Distribution

  • 00887517992963 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 11x18x55mm
Nuvasive, Inc.
6011855P2
In Commercial Distribution

  • 00887517992949 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 11x18x50mm
Nuvasive, Inc.
6011850P2
In Commercial Distribution

  • 00887517992932 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 11x18x45mm
Nuvasive, Inc.
6011845P2
In Commercial Distribution

  • 00887517992925 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 9x18x60mm
Nuvasive, Inc.
6009860P2
In Commercial Distribution

  • 00887517992918 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 9x18x55mm
Nuvasive, Inc.
6009855P2
In Commercial Distribution

  • 00887517992901 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 9x18x45mm
Nuvasive, Inc.
6009845P2
In Commercial Distribution

  • 00887517992888 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 11x22x45mm
Nuvasive, Inc.
6511245P2
In Commercial Distribution

  • 00887517993564 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 9x22x60mm
Nuvasive, Inc.
6509260P2
In Commercial Distribution

  • 00887517993557 ()


  • Polymeric spinal interbody fusion cage
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