BEUDAMED
    8 results · 22ms · 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

    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

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 11, 2013

    RIATA ST ACTIVE FIXATION

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

    CONQUEST PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·July 15, 2014