BEUDAMED
    7 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.

    DANIEL ORTHO BED LIFT AC

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Puritan Bennett 980 Ventilator System

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    URINE COLLECTION BAG TYPE 1505V

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

    PURITAN BENNETT 980 SERIES VENTILATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC/COVIDIEN·Product code CBK·September 17, 2025

    ANGIO-SEAL VASCULAR DEVICE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·June 2, 2014

    COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 8, 2010

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·December 10, 2012