BEUDAMED
    4 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 2, 2023

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·February 5, 2014

    SHORT DRIVER RMAS

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·November 7, 2012

    UNKNOWN SUTURE PRODUCT

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAN·August 30, 2010