BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    PHASE PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    TaqPath™ COVID-19, Flu A, Flu B, RSV Select Negative Control

    FDA UDI
    LIFE TECHNOLOGIES CORPORATION·10190302019002·Component 3 of 4 of A56123 (Applied Biosystems™...

    RIVER- 1 ELECTROCARDIOGRAPH (ECG) RECORDER AND TRANSMITTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Pall QPoint Water Filter Capsule (Shower), Pall QPoint Water Filter Capsule (Faucet)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TOTAL ASR ACET IMP SIZE 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 10, 2012

    TOTAL ASR FEM IMP SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 10, 2012

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 8, 2021

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 23, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·December 20, 2010

    OCULIGHT GL LASER

    FDA Adverse Event
    Malfunction ·IRIDEX CORP.·Product code GEX·November 30, 2012