BEUDAMED
    9 results · 35ms · 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.

    WATCHCHILD

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756571203·BI-LAP CHEST TRAY

    YRNSORTIP OXIMANOMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SHILEY DISPOS. TEMP. PROBES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KNEE IMPLANT-TIBIA INSERT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 6, 2024

    ULTHERA

    FDA Adverse Event
    Injury ·ULTHERA, INC.·Product code OHV·June 10, 2014

    SETROX S 45

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·December 21, 2012

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·November 3, 2010

    GYC-1000

    FDA Adverse Event
    Malfunction ·NIDEK CO., LTD.·Product code HQF·June 18, 2015