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

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    Filters FDA Adverse Event ×

    CM DRIVE IMPLANT 4.3X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·May 17, 2018

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    JUMAO MEDICAL EQUIPMENT·Product code IOR·March 19, 2013

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code DQX·March 9, 2011

    HYDRATOME RX SPHINCTEROTOME

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·March 11, 2008

    HIGH CAPACITY NARROW INTRAMEDULLARY TIP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FQH·September 25, 2023

    HIGH CAPACITY NARROW INTRAMEDULLARY TIP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FQH·September 25, 2023

    UNKOWN BF GLENOIOD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·April 25, 2022

    UNKNOWN BF HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·April 25, 2022

    HIGH CAPACITY NARROW INTRAMEDULLARY TIP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FQH·September 25, 2023

    HIGH CAPACITY NARROW INTRAMEDULLARY TIP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FQH·September 25, 2023