BEUDAMED
    10 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Eu Mdr ×

    CORE1/REBORN Abutment

    Device
    EU MDR · Eu Md Class 2b ·Cybermed Inc.,·Not intended for eu market

    CORE D Guide KIT

    Device
    EU MDR · Eu Md Class 1 ·Cybermed Inc.,·Not intended for eu market

    CORE Drill

    Device
    EU MDR · Eu Md Class 2a ·Cybermed Inc.,·Not intended for eu market

    OnDemand3D

    Device
    EU MDR · Eu Md Class 2a ·Cybermed Inc.,·No longer on the market

    : CORE1/REBORN Implant Fixture

    Device
    EU MDR · Eu Md Class 2b ·Cybermed Inc.,·Not intended for eu market

    CORE1/REBORN Abutment

    Basic UDI-DI
    EU MDR · Eu Md Class 2b ·Cybermed Inc.,·1 device

    CORE D Guide KIT

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Cybermed Inc.,·1 device

    CORE1/REBORN Surgical Instrument

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Cybermed Inc.,·1 device

    OnDemand3D

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Cybermed Inc.,·1 device

    CORE1/REBORN Implant - Fixture

    Basic UDI-DI
    EU MDR · Eu Md Class 2b ·Cybermed Inc.,·1 device