BEUDAMED
    6 results · 22ms · 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.
    Filters Regulation: Us FDA ×

    LSPI AUTOMATIC VENTILATOR, MODEL AV3000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEROYAL ELECTROSURGICAL PENCIL, ROCKER STYLE WITHOUT HOLSTER, DEROYAL ELECTROSURGICAL PENCIL, BUTTON STYLE WITHOUT HOLST

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ESA PLASMA FREE METANEPHRINE ANALYSIS KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CLINITRON RITEHITE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code INX·April 3, 2014

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·January 25, 2013

    UNKNOWN ZIMMER KNEE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·December 14, 2010