BEUDAMED
    6 results · 21ms · 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 ×

    HEARTMATE II LVAS

    FDA Adverse Event
    Death ·THORATEC CORP.·Product code DSQ·April 7, 2014

    MODEL 3000 30ML LOW FLOW PUMP

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF - RAYNHAM·Product code LKK·September 26, 2012

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·July 13, 2010

    BIPLATE SCHAEDLER/SCHAED KV 5% SB 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·June 25, 2021

    BD BBL¿ SCHAEDLER K-V AGAR WITH 5% SHEEP BLOOD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·August 2, 2021

    BIPLATE SCHAEDLER/SCHAED KV 5% SB 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·July 1, 2021