BEUDAMED
    4 results · 20ms · 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 ×

    400 DENTAL NDL 30SH

    FDA Adverse Event
    Injury ·COVIDIEN·Product code DZM·October 17, 2019

    PLUM A+ DRIVER ED 2

    FDA Adverse Event
    Malfunction ·HOSPIRACOSTA RICA LTD.·Product code FRN·February 10, 2014

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·November 14, 2012

    FLEXICAP DISCONNECT CAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 13, 2010