BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P

    FDA 510(k)
    FDA Class 2 ·General Hospital

    F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DAYSTAR SURG. LIGHT 9100 & ORBITER 9110

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NEXGEN CR FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code MBH·February 19, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 31, 2014

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 27, 2011

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·July 24, 2024

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·February 15, 2024

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·April 17, 2025