BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    K012364

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·February 3, 2015

    COMFORT

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025

    COMFORT

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025

    CADD CASSETTE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·September 27, 2024

    CODMAN EXT DRAINAGE SYSTEM III WITHOUT VENT CATH

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC·Product code JXG·March 20, 2013

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·March 9, 2011

    I-STAT CHEM8+ CONTROL, LEVEL 3

    FDA Adverse Event
    Other ·ABBOTT POINT OF CARE INC.·Product code JJE·March 11, 2008

    REAMER HEAD F/RIA 2 Ø10

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·February 26, 2024