BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    SYSMEX CC-130

    FDA 510(k)
    FDA Class 2 ·Hematology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707028833·WEB 1ST MOLAR BANDS n.UL 5

    Hi-Pull

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573024056·HI-PULL STRAP BLUE LARGE

    Orthopantomograph™ OP 3D LX

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPIOX CARDIOTOMY RESERVOIR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·May 23, 2014

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 10, 2012

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018