BEUDAMED
    7 results · 19ms · 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 ×

    CORE DYNAMICS' LAPAROSCOPIC SMOKE ELIMINATOR

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

    ACL SMART System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRUGRAFT BGS SYRINGE, MODEL 600-041

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 11, 2016

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 21, 2013

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 30, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2014