BEUDAMED
    100 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OLSEN ELECTROSURGICAL INC.

    FDA Adverse Event
    Malfunction ·OEI·Product code GEI·August 23, 1999

    AVANCE CS2

    FDA Adverse Event
    Injury ·DATEX-OHMEDA, INC.·Product code BSZ·March 25, 2022

    AVANCE

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA INC·Product code BSZ·February 1, 2022

    ELUTIA WOUND DRAIN

    FDA Adverse Event
    Malfunction ·BACTERIN INTERNATIONAL INC.·Product code OEI·May 15, 2014

    BARD CHANNEL DRAIN, 19 FR. ROUND HUBLESS FULL FLUTED, SILICONE.

    FDA Adverse Event
    C.R. BARD, INC.·Product code OEI·November 3, 2017

    ELUTIA

    FDA Adverse Event
    Malfunction ·BACTERIN INTERNATIONAL INC.·Product code OEI·February 26, 2013

    MEDTRONIC VENTRICLEAR II VENTRICULAR DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROLOGICAL TECHNOLOGIES·Product code OEI·March 24, 2015

    EXPEL¿ MULTO-PURPOSE DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OEI·September 26, 2017

    XENMATRIX AB

    FDA Adverse Event
    Death ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code PIJ·April 3, 2025

    BEI BEI KN95

    FDA Adverse Event
    Injury ·BEI BEI SAFETY CO LTD.·Product code MSH·April 30, 2020

    *

    FDA Adverse Event
    Other ·DEI·Product code HFW·March 18, 1999

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION-HOPKINS·Product code MED·July 1, 2014

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·July 30, 2014

    BEI MEDICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP·Product code MNB·October 17, 2003

    BEI MEDICAL SYSTEMS CO

    FDA Adverse Event
    Injury ·BEI MEDICAL SYSTEMS CO.·Product code MND·October 30, 2002

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·November 29, 2012

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·January 23, 2014

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·October 17, 2012

    HYDRO THERMABLATOR KIT

    FDA Adverse Event
    Malfunction ·BEI MEDICAL SYSTEMS·Product code MNB·January 15, 2002

    HYDROTHERMAL ABLATOR

    FDA Adverse Event
    Other ·BEI MEDICAL SYSTEMS·Product code MNB·September 16, 2002