BEUDAMED
    4 results · 19ms · 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 ×

    ULITIMUM EV INTRODUCER, 19F, 30CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code DYB·April 18, 2014

    LNEXGEN LPS-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code NJL·October 5, 2012

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·May 19, 2015

    ALLOFIT ALLOCLASSIC SHELL 52/I I

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·December 11, 2018