BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LenSx Laser System (8065998162)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    RHEUMADX LATEX AGGLUTINATION RHEUMATOID

    FDA 510(k)
    FDA Class 2 ·Immunology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 5, 2013

    ENTERRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LNQ·December 28, 2010

    FORTIFY VR, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 18, 2014