BEUDAMED
    6 results · 24ms · Sources: EU EUDAMED, US FDA

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    PE 501 PC-ECG MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LAPORT

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

    BEACON Caresystem Model 00002144

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    S-ROM*SLEEVE PRX ZTT, 18F-LRG

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code LPH·March 7, 2013

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·February 15, 2011

    KAPPA 700 DR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NVZ·August 8, 2014