BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code LWR·July 30, 2008

    6000008-1997-00030

    FDA Adverse Event
    Malfunction ·Product code GCY·February 13, 1997

    AP402-01 HCR - MICROBORE YELLOW MARKED WITH NON-VENTED SPIKE

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD.·Product code FPA·March 22, 2016

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·May 6, 2025

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·March 12, 2013

    PORTEX 8.0MM SUCTIONAID TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTL, LTD.·Product code JOH·February 17, 2011

    THERMACARE BACK AND HIP

    FDA Adverse Event
    Injury ·PROCTER & GAMBLE·Product code IMD·February 12, 2008

    POWERLED TM

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·January 12, 2026

    PULSAR 2 GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY·Product code GEI·March 15, 2016

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·January 26, 2025