BEUDAMED
    9 results · 32ms · Sources: EU EUDAMED, US FDA

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    ANESTHESIA CONDUCTION NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEKA MOTUS AX

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

    ASCENT PIT AND FISSURE SEALANT, MODEL 006-00019

    FDA 510(k)
    FDA Class 2 ·Dental

    6.5CM ADULT CRANI ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 13, 2014

    SCORPIO-FLEX CR TIBIAL TRIAL

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·December 22, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 15, 2013

    DEKA MOTUS AX

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 25, 2018

    DEKA MOTUS AX

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·March 9, 2023

    DEKA MOTUS AX

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·February 6, 2024