BEUDAMED
    7 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.

    DSL ACTIVE 17A-OH PROGESTERONE RIA (DSL 5000)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ALL FLOW PULMONARY FUNCTION FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Disposable Pressure Manometer (DPM)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    C-CASSETTE MEDI RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·August 24, 2023

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 21, 2013

    MINICAP DISCONNECT W

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CUERNAVACA·Product code KDI·December 30, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2014