BEUDAMED
    11 results · 27ms · 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.

    IMPAX 5000

    FDA 510(k)
    FDA Class 1 ·Radiology

    UROLAB JANUS

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

    YD STRIP GP U20

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·July 16, 2014

    BD VACUTAINER® SINGLE USE HOLDER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·December 6, 2017

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·January 11, 2013

    FOUNDATION KNEE INSTRUMENT

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code HWA·November 23, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·July 15, 2014

    ECHOTIP ULTRA ULTRASOUND ASPIRATION NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·November 19, 2010

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·July 29, 2014

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·September 17, 2014