BEUDAMED
    3 results · 26ms · 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 ×

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 5, 2014

    M2A MAGNUM TRISPIKE CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 3, 2012

    FLIMM FISHTER DIRECTIONAL STROKING PERCUSSOR

    FDA Adverse Event
    Injury ·GENERAL PHYSIOTHERAPY INC.·Product code BYI·July 20, 2010