BEUDAMED
    4 results · 24ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    PHILIPS LIFELINE GOSAFE WIRELESS COMMUNICATOR

    FDA Adverse Event
    Malfunction ·PHILIPS LIFELINE·Product code ILQ·May 27, 2016

    EB010, VOYANT 5MM FUSION, 37CM 6/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL·Product code GEI·July 25, 2015

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·December 23, 2010

    ERBE VIO 200 S

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·July 7, 2014