BEUDAMED
    9 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ARCAD EXPRESS

    FDA Adverse Event
    Injury ·NOVASTEP·Product code JDR·June 26, 2019

    LAMITRODE TRIPOLE 16C

    FDA Adverse Event
    Injury ·ST. JUDE MED - NEUROMODULATION·Product code GZB·October 15, 2014

    SYSTEM, PERITONEAL AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 20, 2013

    NX3 DUAL CURE CLEAR

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·July 27, 2011

    PEN NEEDLE 32GX4MM 14 PACK

    FDA Adverse Event
    Malfunction ·EMBECTA MEDICAL DEVICES (SUZHOU) CO., LTD., CHINA·Product code FMI·January 15, 2026

    PERCEVAL PLUS SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Death ·CORCYM S.R.L.·Product code LWR·April 10, 2025

    PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE

    FDA Adverse Event
    Injury ·CORCYM S.R.L.·Product code LWR·February 25, 2025

    PERCEVAL PLUS SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Malfunction ·CORCYM S.R.L.·Product code LWR·March 27, 2025

    PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE

    FDA Adverse Event
    Injury ·CORCYM S.R.L.·Product code LWR·January 12, 2025