BEUDAMED
    8 results · 21ms · 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 ×

    GYDER® Hip System

    FDA 510(k)
    FDA Class 2 ·Neurology

    VASCON POLARIS GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GE333 Blood Glucose Monitoring System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CARDIOMEMS PATIENT ELECTRONIC SYSTEM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code MOM·October 8, 2020

    CARDIOMEMS PATIENT ELECTRONIC SYSTEM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code MOM·October 30, 2020

    MICROPUNCTURE TRANSITIONLESS ACCESS SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DYB·August 25, 2011

    OMNILINK ELITE PERIPHERAL STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIO·November 11, 2014

    INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 23, 2013