BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BARD COMPOSIX KUGEL HERNIA PATCH 10"X 13"

    FDA Adverse Event
    Injury ·DAVOL·Product code FTL·August 18, 2006

    0010207 COMPOSIX KUGEL OVAL 10 X 13

    FDA Adverse Event
    Injury ·DAVOL, INC. (RI)·Product code FTL·December 20, 2002

    BARD COMPOSIX KUGEL HERNIA PATCH

    FDA Adverse Event
    Injury ·DAVOL, INC.·Product code FTM·December 19, 2002

    S-ROM*SLEEVE PRX ZTT, 20B-SML

    FDA Adverse Event
    Injury ·DEPUY (IRELAND) 9616671·Product code LPH·March 19, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 1, 2011

    POLYFLUX LR CAPILLARY DIALYZER

    FDA Adverse Event
    Malfunction ·GAMBRO DIAYLZATOREN GMBH·Product code MSF·March 10, 2008

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Death ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·March 20, 2015

    SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·December 27, 2024

    PRODIGY LG STAT SHT LT 12.0MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 2, 2016

    PRODIGY LG STAT LNG LT 13.5MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·June 3, 2018

    EXTENDEVAC W/ COATED BLADE, 10FT TUBING, HOLS

    FDA Adverse Event
    Malfunction ·IC MEDICAL INC·Product code GEI·May 5, 2015