BEUDAMED
    7 results · 33ms · 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.

    URIC ACID REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code KNK·April 15, 2011

    SYNCHRON CX4/CX5 CLINICAL CHEMISTRY ANALYZER REAGE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SCANNER, COMPUTERIZED TOMOGRAPHIC

    FDA 510(k)
    FDA Class 2 ·Radiology

    QV-9000 UNIVERSAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 21, 2012

    QUATTRODE 3/6 PERCUTANEOUS LEADS

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·October 19, 2010

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·February 20, 2014