BEUDAMED
    10,000 results · 389ms · Sources: EU EUDAMED, US FDA

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    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·July 22, 2018

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code GEI·July 11, 2018

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·April 2, 2025

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·April 2, 2025

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·May 28, 2025

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code GEI·May 30, 2025

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·May 8, 2025

    ACL ACC BAYPN W/EYE .094X14" *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code NBH·April 10, 2025

    1.5X4MM HT SD X-DR SCREW EA

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·September 15, 2016

    1.5X4MM HT SD X-DR SCREW EA

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·September 15, 2016

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·May 28, 2025

    1.5X3.5MM HT SD X-DR SCREW EA

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·September 14, 2016

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·May 8, 2025

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·May 28, 2025

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·June 10, 2025

    PUMP, MEDFUSION, MDL 3500, V6 1/EA

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FRN·June 16, 2025

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·April 21, 2025

    PAED. TRACHEOSTOMY TUBE 4.5MM UNCUFFED 1/EA

    FDA Adverse Event
    Malfunction ·SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.·Product code JOH·April 3, 2025

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·May 28, 2025

    VAPR S90 4.0MM W/INTEGR HDP -EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·April 2, 2025