BEUDAMED
    7 results · 17ms · 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.

    LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EX

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PerioLase Nd:YAG Pulsed Dental Laser System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    990

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 4, 2014

    CAROTID WALLSTENT MONORAIL ENDOPROTHESIS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIM·October 26, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 21, 2012

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020