BEUDAMED
    29 results · 21ms · Sources: EU EUDAMED, US FDA

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    BIOSIGN FLU A + B, STATUS FLU A & B

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Oticon

    FDA UDI
    Oticon A/S·05707131257710·H15, BTE 13 WL 100 STG

    MINI L.E.D., MODEL: MINI L.E.D., MODEL SMARTLITE MINI

    FDA 510(k)
    FDA Class 2 ·Dental

    BIPAP AVAPS VENTILATORY SUPPORT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FLEXIMA CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFA·July 15, 2011

    FLEXIMA CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFA·July 15, 2011

    FLEXIMA CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFA·July 15, 2011

    BIPAP A30

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

    BIPAP ST

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

    BIPAP ST

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

    BIPAP AVAPS

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

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 3, 2022

    BIPAP A30

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

    BIPAP AVAPS

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

    BIPAP ST

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

    BIPAP A30

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

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 16, 2022

    BIPAP AVAPS

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

    BIPAP ST

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

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 29, 2013