BEUDAMED
    7 results · 38ms · Sources: EU EUDAMED, US FDA

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    POSSIS MYOCARDIAL SUTURELESS LEAD

    FDA Adverse Event
    Injury ·POSSIS MEDICAL, INC.·Product code LWS·November 14, 1998

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·November 29, 2024

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013

    TOTALCARE BARIATRIC

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC·Product code FNL·February 22, 2011

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 21, 2008

    GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 4+ R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·February 7, 2022

    LACTOSORB 14 MM RAPIDFLAP CLAMP

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code JEY·July 6, 2016