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

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    SUPER STAPLE(TM) CLASSIC

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ArgenZ ST 98x12 ML C3

    FDA UDI
    ARGEN CORPORATION, THE·D818123363·Dental porcelain/ceramic restoration kit

    ZEUS ELISA HSV GC-I IGG TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ANGIOJET SOLENT DISTA THROMBECTOMY SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MONOPLUS VIOLET 1(4)150CM HRC40S LOOP(M)

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·April 5, 2024

    SENSITHERM PROBE

    FDA Adverse Event
    Injury ·FIAB S.P.A.·Product code FLL·July 10, 2023

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORP., ASHITAKA·Product code DQX·June 10, 2011

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008