BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    LIMELIGHT

    FDA 510(k)
    FDA Class 2 ·Dental

    ASSURE PRO BLOOD GLUCOSE MONITORING SYSTEM, MODEL 460001

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Axeo 3 Patient Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TURBO-JECT POWER INJECTABLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LJS·December 18, 2017

    SPRINT QUATTRO

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·February 9, 2013

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·July 23, 2014

    RENAL - DISPOSABLE

    FDA Adverse Event
    Malfunction ·Product code FKX·January 7, 2011