BEUDAMED
    6 results · 18ms · 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 ×

    MYCOAKT M. TUBERCULOSIS CUULTURE ID KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ArgenIS Titanium Abutments

    FDA 510(k)
    FDA Class 2 ·Dental

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS INC.·Product code LZG·January 18, 2013

    CONTINU-FLO SOLN. SET, 3 LUERACTIVATED VALVES

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FPA·December 30, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 17, 2014