BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    AGC V2 REVISION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984054·anteriors; shade A2; mould R 60

    MODIFICATION OF THE CEDIA DIGOXIN ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    5.0 MHZ ARRAY INTRAVAGINAL TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Radiology

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·February 28, 2013

    STERLING SL BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·February 10, 2011

    4MM COARSE DIAMOND BALL

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HSZ·December 18, 2013