BEUDAMED
    3 results · 14ms · 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 Status: Malfunction ×

    TX1 TISSUE REMOVAL SYSTEM - MICROTIP

    FDA Adverse Event
    Malfunction ·TENEX HELTH·Product code LFL·February 24, 2014

    MOOG CURLIN 1.2 MICRO IV TUBING SET 340-4128

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES·Product code FPA·November 12, 2010

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 30, 2012