BEUDAMED
    7,243 results · 69ms · Sources: EU EUDAMED, US FDA

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    VC10 PUMP, 115 V

    FDA Adverse Event
    Injury ·GYRUS MEDICAL INC.·Product code JCX·June 12, 2007

    DISPOSABLE FALOPE-RING BAND APPLICATION KIT

    FDA Adverse Event
    Malfunction ·GYRUS MEDICAL INC.,·Product code KNH·June 18, 2009

    LYONS DISSECTING FORCEPS

    FDA Adverse Event
    Other ·GYRUS MEDICAL INC.·Product code GEI·September 23, 2011

    GYRUS ACMI INC.

    FDA Adverse Event
    Malfunction ·Product code GEX·June 15, 2010

    GYRUS ACMI, INC

    FDA Adverse Event
    Malfunction ·GYRUS ACMI INC.·Product code GEI·June 24, 2009

    GYRUS ACMI, INC

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code KNQ·June 17, 2024

    GYRUS ACMI, INC

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code KNQ·March 18, 2024

    GYRUS ACMI, INC.

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC·Product code GEI·July 22, 2013

    ROTATING CONT. FLOW RESECTOSCOPE INNER SHEATH

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code FED·June 7, 2010

    DISPOSABLE FALOPE-RING BAND APPLICATOR KIT

    FDA Adverse Event
    Injury ·GYRUS MEDICAL, INC.·Product code KNH·April 2, 2013

    OLYMPUS FLEXIBLE SURGICAL INSTRUMENTS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code KNW·March 15, 2011

    OLYMPUS RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·October 29, 2010

    OLYMPUS RESECTION SHEATH

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP·Product code FED·October 21, 2011

    VALVE IN CARTRIDGE, 5MM

    FDA Adverse Event
    Injury ·Product code NJK·November 27, 2020

    OLYMPUS HF RESECTION ELECTRODES

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·May 6, 2011

    OLYMPUS HIGH FREQUENCY RESECTION ELECTRODE

    FDA Adverse Event
    Other ·OLYMPUS WINTER & IBE GMBH·Product code JOS·July 14, 2010

    ACCUTRAC (TM) SINGLE-USE HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEX·February 28, 2018

    OLYMPUS OES CYSTONEPHROFIBERSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAJ·August 26, 2010

    SINGLE USE ASPIRATION NEEDLE

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code FCG·May 31, 2024

    DEPLOYMENT CATHETER AND LOADER, 2.6

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code OAZ·May 13, 2023