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

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    VITEK 2 AST - YEAST FLUCONAZOLE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814756·GENUMEDI EXTRA WIDE SAND SIZE VII

    Oticon

    FDA UDI
    Oticon A/S·05707131264688·RIA PRO, KIT 312 DIR 85 L V BE

    WOODWAY USA, INC.

    FDA registration
    WOODWAY USA, INC.·1 product·🇺🇸 United States

    MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODELS IR1DA1-2, IR1DE1-2

    FDA 510(k)
    FDA Class 2 ·General Hospital

    POSEY BED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 22, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 18, 2015

    PENUMBRA SYSTEM JETD REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·May 8, 2019

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 30, 2015

    PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·June 14, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 26, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    CONVECTIVE PATIENT WARMER

    FDA Adverse Event
    Malfunction ·STRYKER CORP DBA GAYMAR·Product code DWJ·May 12, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 1, 2014

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 9, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·September 9, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·September 16, 2015

    PENUMBRA SYSTEM 4MAX REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 30, 2015