BEUDAMED
    34 results · 24ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO: MODIFIED USS POLYPROPYLENE SUTURE

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

    ULTRASTIM ELECTRODE, MODEL US4040

    FDA 510(k)
    FDA Class 2 ·Neurology

    SNOW LOTUS POWDER FREE LATEX EXAMINATION GLOVES WITH A PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MARY HITCHCOCK HANOVER NH 1

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·November 7, 2012

    CONTOUR THREAD

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·February 15, 2008

    MADIGAN ARMY TACOMA WA 1

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

    CONTOUR THREAD OR CONTOUR THREADS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·February 12, 2013

    UNIV OF VA CHARLOTTESVILLE VA1

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

    CONTOUR THREAD OR CONTOUR THREADS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAP·September 16, 2008

    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

    DIDECO COMPACTFLO EVO

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

    CARELINK

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·April 10, 2013

    RIATA ACTIVE FIXATION LEAD

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

    CAPSUREFIX

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·April 12, 2011

    CONTOUR THREAD OR CONTOUR THREADS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·September 23, 2009

    UNIV OF CHARLOTTESVILLE VA1

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