BEUDAMED
    8 results · 25ms · 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.

    ESOPHAGEAL STETHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Modulus

    FDA UDI
    Nuvasive, Inc.·00195377050038·Modulus ALIF HL Trial, 6x42x32mm 25°

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982193·posteriors; shade D3 light; size XL; lower jaw

    QUICKPAD (ALCOHOL SWABS)

    FDA 510(k)
    FDA Unclassified ·Unknown

    S-Line

    FDA 510(k)
    FDA Class 2 ·Dental

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION INC·Product code DRM·January 25, 2013

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FPA·August 5, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·January 18, 2011