BEUDAMED
    4 results · 28ms · 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 ×

    LEEP AUVARD SPECULUM LG

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HDF·July 1, 2022

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·November 30, 2010

    UNIFY CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·July 2, 2014

    CXDI CONTROL SOFTWARE NE VER. 1.40.3.0

    FDA Adverse Event
    Malfunction ·CANON, INC.-MEDICAL EQUIPMENT GROUP·Product code MQB·December 6, 2012