BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

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    RECHARGE REPLACE BATTERY PK SPACELABS 4045 MON/DEFIB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M-PM-DISC

    FDA 510(k)
    FDA Unclassified ·Unknown

    EARLOOP PROCEDURE MASK

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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 30, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·December 1, 2010

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·July 15, 2014