BEUDAMED
    3 results · 36ms · 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 ×

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 11, 2013

    AED PRO

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 22, 2010

    ASR TAP SLV ADAP 12/14 -1

    FDA Adverse Event
    Malfunction ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 3, 2014