BEUDAMED
    17 results · 25ms · Sources: EU EUDAMED, US FDA

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    In Reach

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATON TO: STEERABLE GUIDE CATHETER, MODEL SGC01ST

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EUROIMMUN ANTI-CCP ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·March 31, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·June 11, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·May 30, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·March 5, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·June 5, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·January 28, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·July 28, 2025

    RFA GROUNDING PAD

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code ODR·May 22, 2013

    HILL-ROM 100 LOW BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·June 22, 2011

    PLUMSET-DUAL W/CON PP, CAP PORT & CLAVE

    FDA Adverse Event
    Malfunction ·HOSPIRA DE COSTA RICA LTD.·Product code FPA·September 15, 2008

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·September 30, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·May 12, 2025

    CRE PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·January 10, 2025

    SUPERCABLE ISO-ELASTIC SYSTEM

    FDA Adverse Event
    Injury ·KINAMED, INC.·Product code JDQ·July 21, 2015