BEUDAMED
    16 results · 15ms · Sources: EU EUDAMED, US FDA

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    Uriki Test K

    Device
    EU IVDD · Eu Ivd General ·Iki·On the market

    PURIPAD

    Device
    EU MDD · Eu Md Class 1 ·SARL CICRETES·No longer on the market

    PURIPAD

    Device
    EU MDD · Eu Md Class 1 ·SARL CICRETES·No longer on the market

    PURIPAD

    Device
    EU MDD · Eu Md Class 1 ·SARL CICRETES·No longer on the market

    PURIPAD

    Device
    EU MDD · Eu Md Class 1 ·SARL CICRETES·No longer on the market

    PURIPAD

    Device
    EU MDD · Eu Md Class 1 ·SARL CICRETES·No longer on the market

    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

    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