BEUDAMED
    7 results · 35ms · 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.

    PULSESTAR EXERCISE BIKE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PARAGON IMMUNOELECTROPHORESIS REAGENT

    FDA 510(k)
    FDA Class 2 ·Immunology

    ISOTEC DISPOS. PRESSURE TRANSDUCER

    FDA 510(k)

    SYMPHONY

    FDA Adverse Event
    Injury ·SORIN CRM·Product code NVZ·June 10, 2014

    SPEEDBAND SUPERVIEW SUPER 7, INJECTION SPEEDBAND SUPERVIEW SUPER 7, MODELS 4205

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code MND·October 11, 2010

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 10, 2012

    HEARTSTRING III SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code DXC·August 18, 2023