BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    DMI SERIES 90 EXAMINATION TABLE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LATERALIZD HUM CUP DIA 36+6MM

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWS·April 9, 2018

    SOLEO SUNBED

    FDA 510(k)

    ACUSON AL538 TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Radiology

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·April 18, 2018

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 25, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 3, 2013

    STRAIGHT LONG SABER ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·November 5, 2010