BEUDAMED
    8 results · 33ms · Sources: EU EUDAMED, US FDA

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    CATHETER, URETERAL DILATOR

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

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867136014·UNIVERS HUMERAL HEAD 46/17

    UROTECH CATHETER

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

    NATIVE PROTHROMBIN ANTIGEN EIA

    FDA 510(k)
    FDA Class 1 ·Immunology

    UNIVERS HUMERAL HEAD 46/17

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·May 19, 2016

    MONOPOLAR CURVED SCISSORS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 3, 2010

    MATNEU SCR Ø1.5 SELF-DRILL L5 TAN 1U I/C

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code JEY·January 14, 2013

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 3, 2014