BEUDAMED
    7 results · 21ms · 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.

    RESPIFLO

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SYNTHES (USA) PEDIATRIC LCP HIP PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLEXIBLE VISUALIZATION CATHETER

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·June 16, 2006

    5.0 CM SHORT ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 11, 2014

    OT VERIO IQ METER

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

    SCORPIO-FLEX PS TIBIAL TRIAL

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·December 22, 2010