BEUDAMED
    12 results · 22ms · 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 ×

    MALE LUER SLIP 64 CAV.

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·March 19, 2021

    MALE LUER SLIP 64 CAV.

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·April 9, 2021

    MALE LUER ADAPTOR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·May 13, 2021

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·September 13, 2013

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·September 13, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·March 1, 2013

    ASR ACETABULAR IMPLANT 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011

    CARPENTIER-EDWARDS BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code LWR·March 14, 2008

    TALENT

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·July 22, 2013

    VALIANT

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·July 22, 2013

    MEDIAL ROTATION KNEE® LEFT TIBIAL INSERT SIZE 2, 10.5MM

    FDA Adverse Event
    Malfunction ·FINSBURY ORTHOPAEDICS LIMITED·Product code JWH·June 19, 2023

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK INC·Product code BWC·September 4, 2019