BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    SMR Finned Short Stems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131340146·SIYA 2, KIT 312 NFM PB L C001

    BD BBL¿ MGIT¿ MYCOBACTERIA GROWTH INDICATOR TUBES, 7ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·March 20, 2023

    VIGILANT EEG MONITOR, VIGILANT 2.0

    FDA 510(k)
    FDA Class 2 ·Neurology

    BRIDGEPOINT MEDICAL MANTARAY(TM) CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DISPENSER, CEMENT

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KIH·August 8, 2017

    DISPENSER, CEMENT

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KIH·August 8, 2017

    PKS LYONS

    FDA Adverse Event
    Malfunction ·OLYMPUS AMERICA, INC.·Product code GEI·October 3, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·August 4, 2011

    BD KIESTRA IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025