BEUDAMED
    6 results · 26ms · 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.

    T-SCOPE, TELEMETRIC PRECORDIAL STETHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    5000 SERIES ECG ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TUBING HOLDER

    FDA 510(k)

    OPTIFLUX F250NRE DIALYZER

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING·Product code KDI·May 19, 2014

    CARDIOVASCULAR PROCEDURE KIT

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

    SERIES 20000 LEGACY

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOLGY CENTER·Product code HQC·December 20, 2012