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

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    MRI'S ALL SILICONE FOLEY CATHETER TEMPERATURE PROBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Well at Walgreens

    FDA UDI
    WALGREEN CO.·00311917185774·WALG FINGER SPLINT LARGE

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

    OTICAON BTE MODEL E34P

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    APPLIED GAUZE SPONGE 4X4X16 PLY

    FDA 510(k)
    FDA Unclassified ·Unknown

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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

    TRANSEND GUIDEWIRE

    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

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·February 5, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 3, 2011

    BARD

    FDA Adverse Event
    Malfunction ·Product code FPA·July 11, 2014

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