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

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    BIPOLAR GENERATOR MODEL 2352

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

    NEW LUTING CEMENT MATERIAL (NLC)

    FDA 510(k)
    FDA Class 2 ·Dental

    PRE-TIED LOOP SUTURE CANNULA

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ENDOLOOP LIGATURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GEA·December 27, 2018

    OPTIBOND SOLO PLUS

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code KLE·February 6, 2013

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 4, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 21, 2014