BEUDAMED
    7 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.

    OPTIFLEX

    FDA 510(k)
    FDA Class 1 ·Dental

    MACLEE/BOIN MEDICA STERILE NEEDLE/SYRINGE 20ML/CC

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEMBRANE KITS-KC1, CO2 & 02 FOR INSTRUMENT-LAB

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·April 18, 2018

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 25, 2014

    CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·November 5, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·December 20, 2012