BEUDAMED
    5 results · 14ms · 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 ×

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    LOCKING SCREW, FULLY THREADED 5X35 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 8, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014