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 ×

    MODIFICATION TO ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET AND TRAY

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

    Vera

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ASAP WOUND DRESSING GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    SYNERGY

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·February 28, 2013

    MINI-CAP, DISCONNECT W/PVP-1SOLUTION

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·February 9, 2011

    X7000 XENON LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code FSS·August 5, 2014