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.

    #400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    INTELECT MODEL 200

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Lung Vision System

    FDA 510(k)
    FDA Class 2 ·Radiology

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES·Product code LZG·June 9, 2014

    SYNCHRON® LX20 PRO CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·October 26, 2010

    PFC SIGMARP STB TB IN 4 12.5

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code NJL·December 21, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021