BEUDAMED
    18 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    CARDIOSAVE

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 3, 2014

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·July 19, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 20, 2025

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 24, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 30, 2023

    4.0MM TI CERV SELF-RETAIN SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code KWQ·February 11, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 3, 2011

    COAGUCHEK XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·February 19, 2008

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 24, 2023

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·December 10, 2025

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·July 9, 2018

    CARDIOSAVE HYBRID TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 19, 2024

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·August 6, 2025

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 24, 2025

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 8, 2025

    ZILVER 635 VASCULAR SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code NIO·March 11, 2021

    CONMED

    FDA Adverse Event
    Malfunction ·NORTHGATE TECHNOLOGIES INC.·Product code HIF·August 29, 2018

    CD003, 5MM RETRIEVAL SYSTEM, 10/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·October 2, 2019