BEUDAMED
    7 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 ×

    OLYMPUS SUPERVIEW LAPAROSCOPE FOR GENERAL SURGERY

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

    GenCut Core Biopsy System

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    C-PET PLUS IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CADD-LEGACY® PCA AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD INC.,·Product code MEA·March 29, 2016

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP.·Product code MKJ·December 21, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 5, 2013

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·July 17, 2014