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

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    Filters FDA Adverse Event ×

    VIAL SUREPATH COLLECTION KIT 500

    FDA Adverse Event
    Malfunction ·TRIPATH IMAGING, INC·Product code MKQ·August 22, 2023

    VIAL SUREPATH COLLECTION KIT 500

    FDA Adverse Event
    Malfunction ·TRIPATH IMAGING, INC·Product code MKQ·August 22, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 30, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

    VIAL SUREPATH COLLECTION KIT 500

    FDA Adverse Event
    Malfunction ·TRIPATH IMAGING, INC·Product code MKQ·August 22, 2023

    GUARDIA¿ ACCESS EMBRYO TRANSFER CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MQF·November 20, 2017

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·March 19, 2013

    NEUROMONITOR BASIC KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC., MEDOS S.A.·Product code GWM·March 2, 2011

    RIATA ST OPTIM ACTIVE-FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008