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

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    Filters FDA Adverse Event ×

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·March 7, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 8, 2014

    CCU BED W/ SCALE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·January 21, 2011

    DURAL ALPHA INSERT W RIM II/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·March 12, 2019

    DURASUL, ALPHA INSERT, HOODED, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·September 28, 2018

    METASUL, ALPHA INSERT, JJ/28

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·February 4, 2019

    DURASUL, ALPHA INSERT, KK/36

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·March 13, 2018

    COCR HEAD 32/ 0 'M' 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·June 4, 2019

    DURASUL, ALPHA INSERT, LL/36

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·April 29, 2019

    DURASUL, ALPHA INSERT, HOODED, KK/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·June 15, 2018