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

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    K090539

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·February 26, 2026

    BIPAP AUTOSV ADVANCED

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADVANCED

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    DREAMSTATION BIPAP AUTOSV

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code MNS·January 16, 2023

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADV SYSTEM ONE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 21, 2022

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 12, 2026

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code MNS·October 31, 2022

    BIPAP AUTOSV ADVANCED SYSTEM

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·January 28, 2022

    DREAMSTATION BIPAP AUTOSV

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code MNS·November 1, 2022

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code MNS·November 7, 2022

    DREAMSTATION BIPAP AUTOSV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code MNS·March 30, 2022

    DREAMSTATION BIPAP AUTOSV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 30, 2022

    OMNILAB ADVANCED PLUS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code MNS·March 31, 2022

    DREAMSTATION BIPAP AUTOSV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code MNS·March 30, 2022

    NYLON NONABSORBABLE SURGICAL SUTURES, USP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TIPOWER POWERDRIVE AND RIMPOWER X & SX

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VKMO 78000 3 QUADROX-I HMO 70000+VHK7000

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 25, 2015