BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·August 2, 2012

    SENSOR MODULE LEVEL/BUBBLE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·May 11, 2012

    ACCESSORIES

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code DQX·March 20, 2025

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 11, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·January 10, 2011

    HL WMR 3. 5X5 W/TAB 25/B 100/C

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS LUDLOW·Product code MPO·July 16, 2014

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·January 6, 2012

    S5 BUBBLE DETECTOR SENSOR 3/16''

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code KRL·February 25, 2022

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·January 6, 2012