BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    VITA YZ Multi Translucent

    FDA 510(k)
    FDA Class 2 ·Dental

    Xrecovery (XR-001)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Vial2Bag Advanced® 20mm Admixture Device

    FDA 510(k)
    FDA Class 2 ·General Hospital

    WALL FLEX COLONIC STENT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code MQR·September 6, 2011

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·November 11, 2014

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 23, 2013

    UNKNOWN BASEPLATE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 18, 2023

    COMP RVS CNTRL 6.5X30MM ST/RST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 18, 2023

    COMP LK SCR 3.5HEX 4.75X20 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 18, 2023

    COMP LK SCR 3.5HEX 4.75X30 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 18, 2023

    COMP LK SCR 3.5HEX 4.75X35 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 18, 2023

    COMP LK SCR 3.5HEX 4.75X25 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 18, 2023

    Minerva-Combi Patient Lift, model ML-30; this lift comes with interchangable passive and active lifting units; Manufactured by Medibo-Technics, Hasseltsebaan 24, 3940 Hechtel-Eksel, Belgium and distributed by MasterCare Patient Equipment, Inc., Hwy 61 West Industrial Park, Columbus, NE 68601

    FDA Recall
    Terminated ·Medibo N.V. Heikant 5 Hanmont, Achel Belgium·Product code FSA·August 4, 2004