BEUDAMED
    6 results · 20ms · 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 ×

    DEBAKEY VASCULOUR-D PROSTHESES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Lucent®

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BODYGUARD PAIN MANAGER INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UNIVERSAL OSCILLATING SAW ATTACHMENT

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL S.A.·Product code GFA·March 10, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 3, 2012

    ITREL 3

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code LGW·July 21, 2010