BEUDAMED
    264 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    SYRINGE 10ML LL S/C 200

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 6, 2019

    GAMBRO LUNDIA PLATE DIALYZER

    FDA Adverse Event
    Malfunction ·CGH MEDICAL·Product code KDI·March 15, 1993

    CENTRYSYSTEM BLOOD TUBING

    FDA Adverse Event
    Malfunction ·CGH MEDICAL·Product code FKB·March 15, 1993

    CENTRYSYSTEM BLOOD TUBING

    FDA Adverse Event
    Malfunction ·CGH MEDICAL·Product code FKB·March 15, 1993

    DIALYZER

    FDA Adverse Event
    Malfunction ·CGH MEDICAL, INC.·Product code FJI·March 1, 1994

    COBE C-3

    FDA Adverse Event
    Malfunction ·CGH MEDICAL, INC.·Product code FII·March 21, 1994

    GAMBRO RENAL PRODUCTS

    FDA Adverse Event
    Malfunction ·CGH MEDICAL INC.·Product code FII·January 10, 2003

    HOSPAL FLAT PLATE DIALYZER

    FDA Adverse Event
    Malfunction ·CGH MEDICAL, INC.·Product code KDI·October 4, 1994

    HOSPAL HEMOSPAL FILTER

    FDA Adverse Event
    Malfunction ·CGH MEDICAL, INC.·Product code FII·November 8, 1994

    HOSPAL HEMOSPAL FILTER

    FDA Adverse Event
    Malfunction ·CGH MEDICAL, INC.·Product code KDI·October 28, 1994

    HOSPAL FLAT PLATE DIALYZER

    FDA Adverse Event
    Malfunction ·CGH MEDICAL, INC.·Product code KDI·October 28, 1994

    SCANMATE A

    FDA Adverse Event
    Malfunction ·DGH TECHNOLOGY, INC.·Product code IYO·December 20, 2016

    DISPOSABLE BLOOD CARTRIDGE

    FDA Adverse Event
    Malfunction ·CGH MEDICAL, INC.·Product code FJK·December 6, 1993

    EMERSON PUMP

    FDA Adverse Event
    Malfunction ·G.H. EMERSON CO.·Product code KDQ·March 21, 1997

    SCANMATE A

    FDA Adverse Event
    Malfunction ·DGH TECHNOLOGY, INC.·Product code ITX·December 20, 2016

    CENTRY SYSTEM 3 CARTRIDGE FOR HEMODIALYSIS

    FDA Adverse Event
    Malfunction ·CGH MEDICAL, INC.·Product code FII·April 7, 1994

    CGH TARGET SLIDES NORMAL METAPHASE

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code PPM·March 26, 2025

    CGH LUNDIA AKPHA 700 (PL-CU/1.3M)

    FDA Adverse Event
    Malfunction ·COBE LABORATORIES·Product code FJG·June 18, 1996

    CGH IC-3L (PL/CU/0.8/L)

    FDA Adverse Event
    Malfunction ·COBE LABORATORIES·Product code FJG·April 24, 1996

    CGH NORMAL MALE METAPHASE SLIDES 2 X 5 SLIDES

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code KEW·April 23, 2010