BEUDAMED
    7 results · 26ms · 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.

    DU PONT ACA METHOTREXATE CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376242156·Tap, Thoracic, 4.5mm

    K-TUBE

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

    CUSTO VIT PULMONARY FUNCTION ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CURRENT DR RF

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 19, 2014

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2015

    ASR 300 SPIKED CUP SIZE 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·October 22, 2010