BEUDAMED
    1,195 results · 40ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    SMARTTOUCH

    FDA Adverse Event
    Malfunction ·MICROPORT CRM S.R.L.·Product code MRM·April 17, 2024

    CDH

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDW·March 29, 2016

    CDH #29

    FDA Adverse Event
    Malfunction ·ETHICON·Product code FHM·December 30, 1992

    LT 270-54, EASYPUMP, 270 ML, 5 ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW, LLC·Product code MEB·November 7, 2012

    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

    PROXIMATE ILS CDH 29

    FDA Adverse Event
    Malfunction ·ETHICON ENDOSURGERY MC #23·Product code GAG·December 31, 1996

    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

    DISPOSABLE BLOOD CARTRIDGE

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

    CENTRY SYSTEM 3 CARTRIDGE FOR HEMODIALYSIS

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

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·January 20, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·February 4, 2022

    CDH 29 ETHICON ENDO STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY·Product code GAG·January 28, 2010