BEUDAMED
    14 results · 53ms · Sources: EU EUDAMED, US FDA

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    PLEURX

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICALS, INC.·Product code KDQ·September 14, 2000

    PLEURX PLEURAL CATHETER

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICALS, INC.·Product code KDQ·January 25, 2001

    CINEMAVISION A/V SYSTEM

    FDA Adverse Event
    Injury ·RESONANCE TECHNOLOGY, INC.·Product code LNH·July 20, 2012

    PLEURX, DENVER BIOMEDICAL

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code KDQ·April 14, 2008

    DENVER PAK W/ SINGLE VALVED SHUNT

    FDA Adverse Event
    Injury ·DENVER BIOMEDICAL, INC.·Product code KPM·November 4, 2003

    DENVER PAK

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICAL, INC.·Product code KPM·January 23, 2007

    PLEURX PLEURAL CATHETER

    FDA Adverse Event
    Other ·DENVER BIOMEDICAL, INC.·Product code DZE·May 10, 2006

    PLEURX PLEURAL CATHETER

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICAL, INC.·Product code KDQ·January 25, 2001

    PLEURX

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICAL, INC.·Product code KDQ·July 25, 2007

    PLEURX PERITONEAL CATHETER

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICAL, INC.·Product code FJS·July 31, 2007

    PLEURX PLEURAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICAL, INC.·Product code KPM·May 2, 2001

    PLEURX PLEURAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICAL, INC.·Product code KPM·May 30, 2001

    PLEURX PLEURAL CATHETER

    FDA Adverse Event
    Malfunction ·DENVER BIOMEDICAL, INC.·Product code KPM·August 21, 2001

    DENVER BIOMEDICAL PLEURX CATHETER

    FDA Adverse Event
    Injury ·DENVER BIOMEDICAL, INC.·Product code KPM·October 17, 2002