BEUDAMED
    6 results · 21ms · 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 Regulation: Us FDA ×

    URI-CATH CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    COPRO 3

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DIGIARC 100AU+

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORP.·Product code MVK·December 21, 2012

    ACRYSOF

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD / HUNTINGTON·Product code HQL·December 10, 2010

    MAQUET HCU30 DEVICE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWC·March 5, 2014