BEUDAMED
    5 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 ×

    G7 LINER

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·April 3, 2018

    FENESTRATED BIPOLAR FORCEPS INSTUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·January 9, 2013

    DYNAGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014

    BINAXNOW COVID-19 AG SELF TEST 4CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·November 5, 2024

    BINAXNOW COVID-19 AG SELF TEST 4CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·April 10, 2025