BEUDAMED
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    SCHOTT AG

    FDA registration
    SCHOTT AG·1 product·🇩🇪 Germany

    ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.

    FDA Recall
    Open, Classified ·Carl Zeiss Meditec AG Rudolf-Eber-Str. 11 Oberkochen Germany·Product code HNQ·March 16, 2022

    EYEMAG LIGHT II

    FDA Adverse Event
    Malfunction ·CARL ZEISS MEDITEC AG (OBERKOCHEN)·Product code KYT·February 7, 2022

    Medical Technology Promedt Consulting GmbH

    Authorized representative
    🇩🇪 Germany·194 Manufacturers·10009 Devices