BEUDAMED
    3 results · 27ms · 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 ×

    ACCU-CHEK ACTIVE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·November 12, 2007

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·October 3, 2012

    FRESENIUS 2008 K2

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE·Product code KDI·November 26, 2013