BEUDAMED
    4 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DEROYAL

    FDA Adverse Event
    Malfunction ·CARWILD CORP·Product code EFQ·June 17, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCO·Product code CBK·February 25, 2013

    MAYFIELD MODIFIED SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA-OHIO, INC·Product code HBL·January 6, 2011

    PEEK CAGE, UNKNOWN TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·February 9, 2021