BEUDAMED
    97 results · 38ms · Sources: EU EUDAMED, US FDA

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    POOL HOIST MKI

    FDA Adverse Event
    Malfunction ·ARJO, LTD.·Product code FSA·October 8, 2002

    APPOSE ULC

    FDA Adverse Event
    Malfunction ·AMERICAN CYANAMID COMP US SURGICAL·Product code GAG·December 10, 2001

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·August 29, 2008

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·May 19, 2020

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 24, 2021

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 19, 2021

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 24, 2021

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 19, 2021

    DGW GUIDEWIRE

    FDA Adverse Event
    Malfunction ·CORDIS CORP. (MIAMI)·Product code MKI·September 8, 2003

    ULTRA-SELECT NITINOL GUIDEWIRE

    FDA Adverse Event
    Injury ·MICROVENA CORPORATION·Product code MKI·February 16, 1994

    DGW .035 FC STR 150CM TEF LLT

    FDA Adverse Event
    Injury ·CORDIS CORP (MIAMI)·Product code MKI·June 7, 2000

    CORDIS

    FDA Adverse Event
    Injury ·CORDIS ENDOVASCULAR·Product code MKI·June 7, 2000

    DGW .035 FC J3MM 260CM TEF

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code MKI·June 22, 2005

    DGW .035 MC J3MM 150CM TEF AMP

    FDA Adverse Event
    Injury ·CORDIS CORPORATION (MIAMI)·Product code MKI·June 29, 2005

    GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BARD INTERVENTIONAL PRODUCTS (C.R. BARD INC.)·Product code MKI·March 7, 1995

    GUIDEWIRE

    FDA Adverse Event
    MEDITECH/BOSTON SCIENTIFIC CORP.·Product code MKI·January 10, 1995

    J-GUIDEWIRE (CENTRAL LINE)

    FDA Adverse Event
    Malfunction ·WALRUS CARDIOVASCULAR PRODUCTS·Product code MKI·March 7, 1995

    DIAGNOSTIC GUIDEWIRE .035 FC J3MM 150CM TEF

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION (MIAMI)·Product code MKI·July 23, 2004

    DGW .035 FC J3MM 150CM TEF

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code MKI·January 24, 2007

    BANDGRIP

    FDA Adverse Event
    Injury ·BANDGRIP INC.·Product code MKY·May 2, 2022