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

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    FIRST MIDCATH CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRANSEND EX 14 GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQX·September 23, 2009

    Lyme B. burgdorferi (IgM) MarStripe Test

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VN415M, VN415B, VO425M, V0425B, 2D-VOG GOGGLES, 2D-VOG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

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    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009

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    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

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    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

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    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

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    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    ONYX

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code MFE·February 21, 2013

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·July 31, 2014

    SETROX S 60

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG,·Product code NVZ·January 21, 2011

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    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010