BEUDAMED
    6 results · 18ms · 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 ×

    HAEMOPHILUS TEST MEDIUM (AGAR)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Optiflux Enexa F500 Dialyzer

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

    DOSE VOLUME HISTOGRAM (DVH) EVALUATOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 24, 2014

    CURLIN 6000

    FDA Adverse Event
    Malfunction ·MOOG·Product code FRN·November 1, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 28, 2012