BEUDAMED
    34 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    OLSEN ELECTROSURGICAL INC.

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

    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

    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

    BEI MEDICAL SYSTEMS

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

    HYDRO THERMABLATOR KIT

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

    HYDRO THERMABLATOR BEI MEDICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP·Product code MNB·October 27, 2003

    BEI MEDICAL SYSTEMS HYDRO THERMABLATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP·Product code MNB·October 27, 2003

    EVOLUTION 3E HP

    FDA Adverse Event
    Malfunction ·EVENT MEDICAL LTD.·Product code CBK·October 22, 2015

    TLIF-C EI 12MM 8DEG 32/12

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·October 21, 2020

    AEI GAUDERER-PORSKY PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TRAY

    FDA Adverse Event
    Malfunction ·BARD INTERVENTIONAL PRODUCTS·March 16, 1992

    SYSTEM 1E PROCESSOR

    FDA Adverse Event
    Malfunction ·STERIS CANADA CORPORATION·Product code NZA·February 22, 2018

    STERIS SYSTEM 1E

    FDA Adverse Event
    Malfunction ·STERIS CANADA CORPORATION·Product code MED·July 12, 2017

    SERV REPL, HD COUPLER, 19.5MM

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code FEI·November 7, 2016

    COUPLER, ZOOM, HD, C-MOUNT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FEI·June 20, 2022

    COUPLER, ZOOM, HD, C-MOUNT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FEI·June 20, 2022

    SCVE REPL, 5:4 HD CPLR, AC

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code FEI·October 13, 2017

    CAMERA COUPLER AC HD 5:4

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code FEI·September 8, 2024