BEUDAMED
    5 results · 20ms · 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

    LOGIC CR TIB INSERT SLOPE +, SZ 1.5, 9 MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·May 6, 2024

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 30, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 2, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 1, 2014