BEUDAMED
    12 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    SYNTHES ANTERIOR CERVICAL PLATE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JDN·May 21, 1997

    CAPTURE-R READY INDICATOR RED CELLS

    FDA Adverse Event
    Malfunction ·IMMUCOR·Product code KSZ·May 18, 2007

    VENTAK MINI+ IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 16, 1997

    TRIMPORT IMPLANTABLE VASCULAR

    FDA Adverse Event
    Malfunction ·GERARD MEDICAL, INC.·Product code LJT·October 2, 1997

    VALLEYLAB ELECTROSURGICAL GENERATOR

    FDA Adverse Event
    Malfunction ·VALLEYLAB, INC.·Product code GEI·July 24, 1998

    CAPTURE-R READY-ID TEST WELLS

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·May 11, 2007

    EXTENSION TUBE, 10 CM LENGTH, 15F/15M

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC SPA·Product code CAH·December 9, 1996

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·August 17, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·July 5, 2013

    BD INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·June 28, 2023

    ELECTRIC DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·March 17, 2014

    AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·October 30, 2013