BEUDAMED
    5,433 results · 31ms · Sources: EU EUDAMED, US FDA

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    MELANOCYTE GROWTH MEDIUM (MGM)

    FDA 510(k)
    FDA Class 1 ·Hematology

    PCA INFUSOR

    FDA Adverse Event
    Injury ·IVAC MEDICAL SYSTEMS·Product code MEA·December 5, 1996

    3M 1812 ASEPTEX MASK

    FDA Adverse Event
    Malfunction ·3M MEDICAL SURGICAL DIV 3M HEALTHCARE·Product code FXX·March 21, 1995

    QUEST 521

    FDA Adverse Event
    Malfunction ·INTELLIGENT PUMP VARIABLE PRESSURE·Product code FRN·March 15, 1993

    ABBOTT PLUM

    FDA Adverse Event
    Malfunction ·ABBOTT / HOSPICE·Product code FRN·May 16, 2005

    FLO-GARD PUMP

    FDA Adverse Event
    FENWAL DIV.·Product code FRN·September 6, 1995

    BAXTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·July 1, 2003

    ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC SCIMED INC·Product code DQO·February 15, 2002

    8F VECTOR X (JL4.0SH)

    FDA Adverse Event
    Death ·MEDTRONIC, AVE, INC.·Product code DYB·March 29, 2002

    ZUMA ZM6F (JL4.0)

    FDA Adverse Event
    Death ·MEDTRONIC AVE, INC.·Product code DQY·March 29, 2002

    MULTI GAS MGM+

    FDA Adverse Event
    Malfunction ·DR`A'GER MEDICAL AG & CO. KGAA·Product code CCK·March 31, 2004

    THERASPHERE®

    FDA Adverse Event
    Death ·BIOCOMPATIBLES UK LTD·Product code NAW·February 15, 2018

    IVAC

    FDA Adverse Event
    Injury ·IVAC CORPORATION·Product code FRN·March 26, 1998

    PC2TX

    FDA Adverse Event
    Injury ·ALARIS MEDICAL SYSTEMS·Product code FRN·December 18, 2002

    PORT-A CATH SINGLE LUMEN 8.5 FR

    FDA Adverse Event
    Injury ·SIMS DELTEC INC·Product code LJT·August 5, 1999

    THERASPHERE®

    FDA Adverse Event
    Injury ·BIOCOMPATIBLE UK LTD.·Product code NAW·February 22, 2018

    THERASPHERE®

    FDA Adverse Event
    Injury ·BIOCOMPATIBLE UK LTD.·Product code NAW·February 22, 2018

    THERASPHERE®

    FDA Adverse Event
    Injury ·BIOCOMPATIBLE UK LTD.·Product code NAW·February 22, 2018

    SYNCHROMED EL

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LKK·December 19, 2007

    ALLEGIANCE PROCEDURE GLOVE

    FDA Adverse Event
    Other ·ALLEGIANCE HEALTHCARE CORP.·Product code LYY·March 14, 1998