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

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    TechCare Trauma

    FDA 510(k)
    FDA Class 2 ·Radiology

    Pulmogine Vibrating Mesh Nebulizer

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AX'S ENDO 04, 06, 08, 2.5, 40 , MODELS 50100206, 50100217, 50100218, 50100230, 50100232

    FDA 510(k)
    FDA Class 1 ·Dental

    VISTA T PULSE GENERATOR

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code DXY·July 8, 1997

    BIPOLAR ENDOCARDIAL LEAD

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code DTB·July 8, 1997

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 2, 2023

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 11, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 9, 2011

    PFC*SIGMA/RD/DOME PAT 3PEG,35

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 23, 2013