BEUDAMED
    62 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    PENCIL, H2K, PUSHBUTTON

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·September 10, 2020

    PENCIL, H2K, PUSHBUTTON

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·November 23, 2020

    PENCIL, H2K, PUSHBUTTON

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·April 13, 2023

    SINGLE USE GUIDWIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code OCY·March 17, 2021

    SINGLE USE BILIARY STENT V

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGE·August 19, 2021

    SINGLE USE 3-LUMEN NEEDLE KNIFE V

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·June 29, 2022

    GONOCHEK-II

    FDA Adverse Event
    Malfunction ·EY LABORATORIES (H.K.) LTD.·Product code GTH·November 10, 1993

    BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code EOQ·December 21, 2022

    TUNNELER 600MM RIGID

    FDA Adverse Event
    Malfunction ·CHRISTOPH MIETHKE GMBH & CO KG·Product code GYK·December 1, 2025

    SHEATH, PERITONEAL INTRODUCER, 46CM - BOX OF 5

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code GYK·May 27, 2020

    CATHETER PASSER, DISPOSABLE, 38 CM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code GYK·March 24, 2017

    CATHETER PASSER 60CM

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code GYK·January 19, 2016

    SHUNT TUNNELER

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES IMPLANTS SA·Product code GYK·August 14, 2012

    PERITONEAL INTRODUCER SHEATHS 70CM

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCICENCS IMPLANTS SA·Product code GYK·September 29, 2016

    CODMAN

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES PRODUCTION CORPORATION·Product code GYK·August 26, 2022

    SHUNT TUNNELER

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES IMPLANTS S.A.·Product code GYK·December 20, 2013

    SHUNT TUNNELER

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCICENCS IMPLANTS SA·Product code GYK·March 3, 2022

    SINGLE USE GUIDWIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code OCY·May 12, 2021

    SINGLE USE 3-LUMEN SPHINCTEROTOME V

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·June 15, 2022

    SINGLE USE 3-LUMEN NEEDLE KNIFE V

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·October 6, 2021