BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    REVEAL INSERTABLE LOOP RECORDER (ILR) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972242·posteriors; shade D3 light; size L; upper jaw

    COR ANALYZER II, MODEL V1.7

    FDA 510(k)
    FDA Class 2 ·Radiology

    DripAssist Plus

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IDENTITY IMPRINT PS

    FDA Adverse Event
    Malfunction ·CONFORMIS, INC·Product code JWH·December 13, 2023

    8.5MM MEDULLARY REAMER HEAD

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·February 21, 2013

    GORE PROPATEN VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·January 20, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014