BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    APR POROUS HA HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973124·posteriors; shade C4; size M; upper jaw

    PEEK Biosolution

    FDA 510(k)
    FDA Class 2 ·Dental

    COLLIMARE COLLIMATOR FAMILY

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·June 27, 2019

    INNER TUBE WITH CERAMIC BEAK

    FDA Adverse Event
    Malfunction ·KARL STORZ GMBH & CO. KG·Product code GCJ·June 5, 2014

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 21, 2013

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·January 28, 2011