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

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    AURIGA QI

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SMARTPIN

    FDA UDI
    Conmed Corporation·10845854014592·SMARTPIN SELF-REINFORCED TECHNOLOGY, Ø1.5 X 70 MM

    SMARTPIN

    FDA UDI
    Conmed Corporation·10845854014599·SMART PIN, DIAMETER 1.5 X 70MM

    HYPERGLIDE AND HYPERFORM OCCLUSION BALLOON SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HNC-127-TRIO NEUROVASCULAR ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    TENDRIL STS

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014

    INVANCE

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTM·May 10, 2013

    UNKNOWN DEPUY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 2, 2011

    EGIA 45 ARTICULATING MED/THICK SULU

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·December 9, 2015