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 ×

    CERAM-ETCH

    FDA 510(k)
    FDA Class 2 ·Dental

    SPECTRUM X-RAY CORP

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDIPART FACE MASK MP-XM

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 6, 2014

    AGILIS NXT LOWE PKG ASSY

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC (AF-MINNETONKA)·Product code DYB·November 29, 2012

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·September 30, 2010