BEUDAMED
    10 results · 26ms · 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 ×

    8010300-2006-00001

    FDA Adverse Event
    Other ·Product code MIA·July 25, 2006

    ARCOS 15X250MM SPL TPR DIST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 7, 2018

    MAGNESIUM

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JGJ·March 8, 2021

    VIRTUOSO VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·February 11, 2011

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    ALIGN RS RETROPUBIC/SUPRAPUBIC URETHRAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code OTN·March 14, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 1, 2011

    TALENT TAA

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR·Product code MIH·June 4, 2013

    TRANSVENE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·December 13, 2010

    PINN MAR +4 10D 36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 29, 2011