BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    ROCHE REAGENT FOR URIC ACID--MODIFICATION

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    JOWIRE NEO'S PTCA CATHETER GUIDEWIRES, MODELS AG141000, AG142000, AG143000, AG141002, AG141010, AG14M060 & AG14M050

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCULIS ACCU21 PMTA MICROWAVE TISSUE ABLATION APPLICATOR

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

    KAPPA 700 SR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·December 13, 2010

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 18, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 14, 2014

    ASAHI PROWATER

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code DQX·June 9, 2019

    ASAHI PROWATER

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code DQX·June 9, 2019