BEUDAMED
    3 results · 28ms · 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 ×

    EDM LUMBAR DRAINAGE KIT, OPEN TIP CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·June 25, 2014

    ACCUSOL K+4 CLEARFLEX 5L (CE MARK)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CASTLEBAR·Product code KPO·November 9, 2010

    HUMIDIFIER 350 CC BUBBLE HUMIDIFIER

    FDA Adverse Event
    Other ·SALTER LABS·Product code CAF·December 27, 2012