BEUDAMED
    6 results · 37ms · 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.
    Filters Regulation: Us FDA ×

    DST-XL

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIQUICHEK ELEVATED CRP CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    HEINE SIGMA 250 & HEINE SIGMA 250 M2

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OT VERIO TEST STRIPS

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

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP.·Product code MKJ·December 21, 2010

    LANCET DEVICE SNSRTR CMFRT EN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 17, 2014