BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    MONOCRYSTANT PH/LES CATHETER, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LEXINGTON MEM W COLUMBIA SC 2

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·October 30, 2013

    SURGITEK GRADUATED URETEROSCOPE (MODEL GU-8)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RECONSTITUTION DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OT VERIO IQ METER

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

    6461500 INFUSOR PUMP (1 LABEL)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 4, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 4, 2014