BEUDAMED
    362 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Eu Mdr ×

    AKZENTA|ONE

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·29 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    ORBIS

    Device
    EU MDR · Eu Md Class 1 ·Akzenta International SA·On the market·28 countries

    abaisses-langue cirêtes

    Device
    EU MDR · Eu Md Class 1 ·SARL CICRETES·Not intended for eu market

    PRONTO CICRETES

    Device
    EU MDR · Eu Md Class 2a ·SARL CICRETES·Not intended for eu market

    PRONTO CICRETES

    Device
    EU MDR · Eu Md Class 2a ·SARL CICRETES·Not intended for eu market

    PRONTO CICRETES

    Device
    EU MDR · Eu Md Class 2a ·SARL CICRETES·Not intended for eu market

    STERIPAD

    Device
    EU MDR · Eu Md Class 1 ·SARL CICRETES·Not intended for eu market

    STERIPAD

    Device
    EU MDR · Eu Md Class 1 ·SARL CICRETES·Not intended for eu market

    STERIPAD

    Device
    EU MDR · Eu Md Class 1 ·SARL CICRETES·Not intended for eu market

    STERIPAD

    Device
    EU MDR · Eu Md Class 1 ·SARL CICRETES·Not intended for eu market