BEUDAMED
    6 results · 28ms · 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 ×

    GLIADIN IGA ELISA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTERVENTIONAL PRODUCTS - GUIDE WIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·March 5, 2013

    VERSA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 7, 2014