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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.
6309255
In Commercial Distribution

  • 00887517305848 ()


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

  • 00887517305824 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x65mm 15°
Nuvasive, Inc.
7161665
In Commercial Distribution

  • 00887517731807 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x60mm 15°
Nuvasive, Inc.
7161660
In Commercial Distribution

  • 00887517731784 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x55mm 15°
Nuvasive, Inc.
7161655
In Commercial Distribution

  • 00887517731760 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x50mm 15°
Nuvasive, Inc.
7161650
In Commercial Distribution

  • 00887517731746 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x45mm 15°
Nuvasive, Inc.
7161645
In Commercial Distribution

  • 00887517731722 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 16x18x40mm 15°
Nuvasive, Inc.
7161640
In Commercial Distribution

  • 00887517731708 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 15x18x65mm 15°
Nuvasive, Inc.
7161565
In Commercial Distribution

  • 00887517731685 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 15x18x60mm 15°
Nuvasive, Inc.
7161560
In Commercial Distribution

  • 00887517731661 ()


  • Polymeric spinal interbody fusion cage
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