BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RUNTHROUGH GUIDE WIRE FOR CARDIAC CATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 26, 2024

    RUNTHROUGH NS

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 9, 2017

    LINOX SD 65/18

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code LWS·September 12, 2011

    PROTEGE

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 29, 2013

    BD MICROLANCE¿ 3 HYPODERMIC NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 12, 2018

    RUNTHROUGH NS

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2018