BEUDAMED
    4 results · 18ms · 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 ×

    TARGET HELICAL ULTRA 3 MM X 8 CM

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR CORK·Product code HCG·June 13, 2014

    LINOX SD 65/18

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code LWS·October 15, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·December 13, 2012

    1.5MM MANDIBLE MESH FOOT B-TYPE FOR CMF DISTRACTOR

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MQN·March 7, 2013