BEUDAMED
    18 results · 22ms · Sources: EU EUDAMED, US FDA

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    Examion X-AQS

    FDA 510(k)
    FDA Class 2 ·Radiology

    FEMORAL HEAD BIOLOX DELTA CERAMIC 12/14 - 28 L

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·February 21, 2024

    BALANCEBACK MOBILE INTUITIVE VNG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    ASPIRE HD FULL-FIELD DIGITAL MAMMOGRAPHY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    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

    ANEURX

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·June 14, 2013

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·July 12, 2011

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 15, 2008

    MONTERIS MEDICAL NEUROBLATE SYSTEM

    FDA Adverse Event
    Malfunction ·MONTERIS MEDICAL CORPORATION·Product code GEX·April 22, 2015

    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