BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    SUTURE CLIP APPLIER/REMOVER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MALDI Biotyper-BD sirius one CA System

    FDA UDI
    Bruker Daltonik GmbH·04251204326359·Biotyper system for clinical use in the USA, wi...

    GE DATEX-OHMEDA AISYS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    K-Shield Advantage Port Access Infusion Set (PAIS)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 22, 2010

    FORTIFY DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014