BEUDAMED
    4 results · 23ms · 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 ×

    SYNCHRON® CK 2 X 400

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CKA·May 10, 2011

    UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code MMI·May 27, 2014

    SPIROS CONNECTOR

    FDA Adverse Event
    Other ·ICU MEDICAL, INC.·Product code FPA·June 1, 2010

    DELTA CER HEAD 12/14 36MM +5

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code KWA·November 15, 2012