BEUDAMED
    3 results · 15ms · 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 Status: Malfunction ×

    DURASUL, ALPHA INSERT, HH/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KWZ·December 14, 2018

    LNOP MP12 PATIENT CABLE

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·May 15, 2015

    FIBER ONE

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER-SILICON VALLEY·Product code GEX·December 7, 2010