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

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    Filters FDA Adverse Event ×

    NO DEVICE

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·February 4, 2025

    SMR REVERSE HUMERAL BODY

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 21, 2022

    PHYSICA FIXED TIBIAL PLATE #3

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HRY·February 13, 2023

    SAPPHIRE M.T INFUSION PUMP

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD.·Product code FRN·November 16, 2015

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, PUERTO RICO, B.V.·Product code MGB·May 14, 2007

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·March 12, 2013

    UNKNOWN PREFILL

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code NZW·February 17, 2011

    BONE WAX 24X2.5G

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code MTJ·October 30, 2019

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·December 21, 2020

    BONE WAX 24X2.5G

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code MTJ·May 7, 2019

    POWERLED TM

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·February 5, 2026

    SMR REVERSE FINNED HUMERAL BODY

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·February 4, 2022

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025