BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·March 12, 2026

    ALLOFT-S ALLOCLASSIC SHL 52/II

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code JDI·March 12, 2019

    FIDELIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code LWS·March 12, 2013

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURUING·Product code LKK·February 24, 2011

    ACUITY CENTRAL MONITORING

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code DSI·February 22, 2008

    ALLOFIT-S ALLOCLASSIC, SHELL WITH POLAR SCREW PLUG, UNCEMENTED, 52/II

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·September 27, 2018

    BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·June 21, 2019