BEUDAMED
    42 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    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

    ALARIS PUMP MODULE

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

    DGW GUIDEWIRE

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

    DGW .035 FC J3MM 260CM TEF

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

    GUIDEWIRE

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

    DGW .035 FC J3MM 150CM TEF

    FDA Adverse Event
    Malfunction ·CORDIS CORP (MIAMI)·Product code MKI·October 12, 2000

    DGFW.035 FC J3MM SS 150CM PTFE

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code MKI·November 28, 2006

    DGW.035 FC R1.5MM 180CM PTFE

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION (MIAMI)·Product code MKI·February 1, 2001

    DGW .035 FC J3MM 150CM TEF

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION (MIAMI)·Product code MKI·May 9, 2003

    CORDIS

    FDA Adverse Event
    Malfunction ·CORDIS·Product code MKI·July 29, 1994

    ACS CATHETER/GUIDEWIRE

    FDA Adverse Event
    Malfunction ·ACS·Product code MKI·July 29, 1994

    GUIDEWIRE

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code MKI·August 29, 1994

    7F STANDARD ATHEROCATH/SUPPORT GUIDEWIRE

    FDA Adverse Event
    Malfunction ·DVI/ACS (GUIDEWIRE)·Product code MKI·July 29, 1994

    DGW. 035 MC J3MM 150CM TEF AMP

    FDA Adverse Event
    Malfunction ·CORDIS CORP (MIAMI)·Product code MKI·December 9, 2004

    MOVEABLE CORE TELFON COATED GUIDEWIRE

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code MKI·July 1, 1993

    PEG GUIDE WIRE

    FDA Adverse Event
    Malfunction ·BARD·Product code MKI·July 17, 1992