BEUDAMED
    19 results · 52ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    SCREENING CELLS TRIO

    FDA Adverse Event
    Other ·GAMMA BIOLOGICALS, INC.·Product code KSZ·March 25, 2002

    GAMMACLONE ANTI-D (MONOCLONAL BLEND)

    FDA Adverse Event
    Malfunction ·GAMMA BIOLOGICALS, INC.·Product code KSZ·November 30, 2006

    SCREENING CELLS TRIO

    FDA Adverse Event
    Other ·GAMMA BIOLOGICALS, INC.·Product code KSZ·July 11, 2002

    GAMMA ANTI-D BLOOD GROUPING REAGENT

    FDA Adverse Event
    Malfunction ·GAMMA BIOLOGICALS INC·Product code KSZ·June 9, 2006

    SCREENING CELLS TRIO

    FDA Adverse Event
    Death ·GAMMA BIOLOGICALS, INC.·Product code KSZ·June 18, 2003

    ANTI-D IGM-IGG (MONOCLONAL BLEND)

    FDA Adverse Event
    Other ·GAMMA BIOLOGICALS, INC.·Product code KSZ·May 27, 2003

    SCREENING CELLS TRIO

    FDA Adverse Event
    Other ·GAMMA BIOLOGICALS, INC.·Product code KSZ·May 1, 2002

    GAMMACLONE ANTI-D (MONOCLONAL BLEND)

    FDA Adverse Event
    Malfunction ·GAMMA BIOLOGICALS, INC.·Product code KSZ·August 4, 2006

    GAMMACLONE ANTI-D MONOCLONAL BLEND

    FDA Adverse Event
    Malfunction ·GAMMA BIOLOGICALS, INC.·Product code KSZ·July 26, 2006

    GAMMACLONE ANTI-D (MONOCLONAL BLEND)

    FDA Adverse Event
    Malfunction ·GAMMA BIOLOGICALS, INC·Product code KSZ·July 31, 2006

    CANCELLO-PURE WEDGE

    FDA Adverse Event
    Injury ·RTI BIOLOGICS·Product code MQV·November 16, 2012

    CANCELLO-PURE WEDGE

    FDA Adverse Event
    Injury ·RTI BIOLOGICES·Product code MQV·November 30, 2012

    CANCELLO-PURE WEDGE

    FDA Adverse Event
    Injury ·RTI BIOLOGICS·Product code MQV·November 16, 2012

    INSPIRE 6 HOLLOW FIBER OXYGENATOR WITH INTEGRATED HARDSHELL VENOUS/CARDIOTOMY

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·February 15, 2019

    INSPIRE 8F HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHELL

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·February 13, 2019

    MENTOR 450ML CPX3 TALL HT CONTOUR PROFILE EXPANDER

    FDA Adverse Event
    Injury ·MENTOR·Product code LCJ·September 20, 2012

    CANCELLO-PURE WEDGE

    FDA Adverse Event
    Injury ·RTI BIOLOGICS·Product code MQV·November 30, 2012

    FORTIVA PORCINE DERMIS

    FDA Adverse Event
    Injury ·TUTOGEN MEDICAL GMBH·Product code FTM·June 19, 2015

    Emergo Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·900 Manufacturers·22100 Devices