BEUDAMED
    3 results · 36ms · 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 ×

    PENUMBRA COIL 400

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·June 19, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·October 20, 2010

    ALLURA XPER FD10

    FDA Adverse Event
    Injury ·PHILIPS HEALTHCARE - BET NETHERLANDS·Product code IZI·December 19, 2012