BEUDAMED
    4 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 ×

    QUIK-COMBO PACING/DEFIBRILLATION/ECG

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL CORP·Product code LDD·March 31, 1998

    RETRACTOR HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code GAD·April 11, 2013

    ACUITY

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·April 12, 2011

    RINGLOC BI-POLAR CUP

    FDA Adverse Event
    Malfunction ·BIOMET, INC.·Product code JDI·May 20, 2008