BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    INTERLIG

    FDA 510(k)
    FDA Class 2 ·Dental

    EASYCUP

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    HEVYLITE HUMAN IGM KAPPA AND HEVYLITE IGM LAMBDA KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    PROSOUND F75 ULTRASOUND SCANNER

    FDA Adverse Event
    Malfunction ·HITACHI ALOKA MEDICAL, LTD·Product code GXX·July 16, 2014

    EXTRACTSCR F/PFNA BLADE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code GFA·May 22, 2013

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN VALLEYLAB·Product code GEI·May 31, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·August 15, 2008

    PEN NDL 32G 4MM 5 BAG 50 BOX SAMPLE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMI·May 5, 2020

    UNK - CAGE/PLATE: SYNFIX EVOLUTION

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OVD·April 21, 2025