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

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    Filters FDA Adverse Event ×

    TREK

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code LOX·December 19, 2024

    TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·March 30, 2012

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ NORTH AMERICA, INC.·Product code LNM·October 17, 2013

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 20, 2013

    SOLETRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·February 2, 2011

    PHOENIX

    FDA Adverse Event
    Other ·GAMBRO DASCO·Product code FID·February 6, 2008

    FEMOSTOP

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS, INC.·Product code MGB·November 21, 2003

    FEMOSTOP

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS·Product code DXC·August 20, 2003

    TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code LOX·October 7, 2020

    NOVOSYN QUICK UNDY 3/0(2)70CM HR26(M)DDP

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·June 24, 2019

    NOVOSYN QUICK UNDY 3/0(2)70CM HR26(M)DDP

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·June 24, 2019

    NOVOSYN QUICK UNDY 3/0(2)70CM HR26(M)DDP

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·June 24, 2019