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

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    SIEMENS FIO2 SENSOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DR 100s

    FDA 510(k)
    FDA Class 2 ·Radiology

    ARK ZONISAMIDE ASSAY, ARK ZONISAMIDE CALIBRATOR, AND ARK ZONISAMIDE CONTRO, MODELS 5022-0001-00, 5022-0002-00, 5022-0003

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 23, 2026

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·May 8, 2026

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·March 25, 2026

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·March 6, 2013

    SYMMETRY 40 OVER-THE-WIRE BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·February 15, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 27, 2026

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 13, 2026

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·March 30, 2026

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 22, 2026

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 22, 2026

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·March 20, 2026

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 30, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·November 24, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 15, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 9, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 4, 2025