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

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    REVEAL PLUS INSERTABLE LOOP RECORDER SYSTEM, MODEL 9526 IMPLANTED RECORDER AND MODEL 6191 PATIENT ACTIVATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    L.P.I. LASER DELIVERY SYSTEM

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

    OSSEODENT SURGICAL KIT

    FDA 510(k)
    FDA Class 2 ·Dental

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 8, 2013

    GMK FEMORAL CUTTING GUIDE

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL, SA·Product code JWH·January 14, 2011

    COBAS 8000 C702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 8, 2014