BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    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

    MENTOR TISSUE EXPANDER

    FDA Adverse Event
    Malfunction ·MENTOR CORPORATION·Product code LCJ·January 17, 2013

    VASOVIEW 6 EVH SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·December 9, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 22, 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