BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    HYDROFLEX HD HYSTEROSCOPIC DISTENTION SYSTEM,MODEL #'S 0025360, 0025370, 0025000

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CORPAK PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE

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

    ULCERCARE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ASCENT SYSTEM-BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·December 28, 2016

    LIBERTY CYCLER

    FDA Adverse Event
    Other ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·June 25, 2014

    ENCORE BALLOON CATHETER INFLATION DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code MAV·February 9, 2011

    TOTAL ASR FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·September 28, 2016