BEUDAMED
    6 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.

    SPQ TEST SYSTEM FOR ALPHA, - ANTITRYPSIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    Cortex Laser System

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

    FULL AUTOMATIC (NIBP) BLOOD PRESSURE MONITOR, MODELS HL888KM, HL888DM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OLYMPUS EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code FDT·May 22, 2014

    BIOCOR STENTED PROCINE HEART VALVE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL BRASIL LTDA.·Product code LWR·November 16, 2012

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 17, 2015