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

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    Filters Regulation: Us FDA ×

    QUANTIA LA(A)

    FDA 510(k)
    FDA Class 2 ·Immunology

    BIPOLAR PENCIL, MODEL 3901-002, 3900-002

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

    MEDTRADE PRODUCTS ALGINATE ISLAND

    FDA 510(k)
    FDA Unclassified ·Unknown

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO.·Product code FGE·November 21, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO.·Product code FGE·November 5, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code FGE·February 20, 2009

    MADIGAN ARMY TACOMA WA 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DWE·December 7, 2009

    UNIV OF VA CHARLOTTESVILLE VA1

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·December 28, 2010

    HCSG MIDWEST REG LEXINGTON KY1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DWE·February 16, 2010

    DIDECO COMPACTFLO EVO

    FDA Adverse Event
    Other ·SORIN GROUP USA ITALIA·Product code DTZ·November 27, 2012

    PENROSE HSP CO SPRINGS CO 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DTZ·April 4, 2007

    UNIV OF VA CHARLOTTESVILLE VA1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DWE·April 20, 2011

    WV UNIV HSP MORGANTOWN WV 1

    FDA Adverse Event
    Other ·SORIN GROUP USA·Product code DTZ·November 10, 2011

    BASIS¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·July 19, 2012

    DIDECO COMPACTFLO EVO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 8, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 8, 2013

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 15, 2011

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO.·Product code FGE·November 4, 2008

    UNIV OF CHARLOTTESVILLE VA1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DTZ·April 21, 2011