BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    DIOMED 25 SURGICAL DIODE LASER, GEN SURG APPLICAT

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

    Damon 3

    FDA UDI
    ORMCO CORPORATION·00889989003604·U4&5L DAMON 3 .022 -7/+2/0

    SYSTEM 7300 PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARTHROBOT(TM) 96 (240 CM) DRAPE WITH 1 STRAP

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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 15, 2015

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-CLONMEL·Product code NIQ·December 3, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 14, 2013