BEUDAMED
    7 results · 59ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    MCKESSON

    FDA Adverse Event
    Injury ·REGULATORY INSIGHT INC.·Product code FOX·January 31, 2017

    LANCE 10 BLADE

    FDA Adverse Event
    Malfunction ·REGULATORY INSIGHT, INC.·Product code GFA·October 18, 2004

    LOKOMAT

    FDA Adverse Event
    Malfunction ·REGULATORY INSIGHT, INC.·Product code IKK·March 22, 2016

    LOKOMAT

    FDA Adverse Event
    Malfunction ·REGULATORY INSIGHT, INC.·Product code IKK·March 22, 2016

    LOKOMAT

    FDA Adverse Event
    Malfunction ·REGULATORY INSIGHT, INC.·Product code IKK·March 22, 2016

    LOKOMATPRO

    FDA Adverse Event
    Malfunction ·REGULATORY INSIGHT, INC. (HOCOMA AG)·Product code IKK·August 3, 2016

    CAREX WEIGHT CAPACITY 300 LB SHOWER STOOL

    FDA Adverse Event
    Injury ·COM-DA HEALTHCARE CO. LTD / REGULATORY INSIGHT INC.·Product code ILS·July 2, 2019