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

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    Filters Regulation: Us FDA ×

    AIS MODULIFT VBR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Cardiovascular Procedure Kit

    FDA UDI
    Terumo Cardiovascular Systems Corporation·50699753464655·

    K133801

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 31, 2024

    TRUSIGNAL R SPO2 PEDITIP SENSOR; TRUSIGNAL R SPO2 PEDITIP SENSOR; TRUSIGNAL R SPO2 PEDITIP SENSOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ATHENA MULTI-LITE RHEUMATOID FACTOR IGM TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 26, 2021

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 27, 2020

    EDWARDS PRIMA PLUS STENTLESS BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 29, 2013

    DEPUY ASR XL FEM IMP SIZE 49

    FDA Adverse Event
    Death ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·October 1, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·June 20, 2011