BEUDAMED
    6 results · 25ms · 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.

    SUPER DUO

    FDA 510(k)
    FDA Class 1 ·Microbiology

    CAPD U.V. GERMICIDAL CONNECTION SYSTEM

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

    primeMidline Catheters

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 24, 2014

    ACCOLADE STEM INSERTER/EXTRACTOR

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·November 3, 2010

    PRONE VIEW CUSHION INSERT

    FDA Adverse Event
    Injury ·MIZUHO OSI·Product code KME·December 26, 2012