BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LOCK

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LPH·September 26, 2024

    DURALENS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·May 4, 2016

    PINNACLE SECTOR II CUP 50MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·May 8, 2014

    MERIT CUSTOM KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code FMF·October 17, 2012

    C-ARM

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD. (GE PRIVATE)·Product code JAA·August 11, 2010

    LINER FOR METAL BACK GLENOID SMALL-R 2

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·November 23, 2020

    SMR GLENOID PEG TT SMALL-R #L

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·June 26, 2019

    SMR GLENOID PEG TT SMALL-R #L

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·March 18, 2022