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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-W+, 9x22x55mm 10°
Nuvasive, Inc.
6309255P2
In Commercial Distribution

  • 00887517993229 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 9x22x45mm 10°
Nuvasive, Inc.
6309245P2
In Commercial Distribution

  • 00887517993205 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 12x18x55mm
Nuvasive, Inc.
6012855P2
In Commercial Distribution

  • 00887517992987 ()


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

  • 00887517992963 ()


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

  • 00887517992925 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 9x18x50mm
Nuvasive, Inc.
6009850P2
In Commercial Distribution

  • 00887517992895 ()


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

  • 00887517992888 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 7x18x60mm
Nuvasive, Inc.
6007860P2
In Commercial Distribution

  • 00887517992871 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 7x18x55mm
Nuvasive, Inc.
6007855P2
In Commercial Distribution

  • 00887517992864 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 13x9x28mm 4°
Nuvasive, Inc.
6041328P2
In Commercial Distribution

  • 00887517679468 ()


  • Polymeric spinal interbody fusion cage
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