BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    CD 3700 SL

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007

    CELL-DYN 3500 SYSTEM WITH IMMATURE RETICULOCYTE FRACTION (IRF), CELL-DYN 3700 SYSTEM WITH IMMATURE RETICULOCYTE FRACTION

    FDA 510(k)
    FDA Class 2 ·Hematology

    CELL-DYN 3700 SL ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019

    BA KIT,WE,P37(90),1',BE,P37,INL,6',STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828136815·BA KIT,WE,P37(90),1',BE,P37,INL,6',STKR

    Neocis Guidance System (NGS)

    FDA 510(k)
    FDA Class 2 ·Dental

    GOAT ANTI-HUMAN ALPHA-1-ANTITRYPSIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    FOLFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·March 6, 2013

    ULTRA-THIN SDS BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code DQY·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014