BEUDAMED
    30 results · 74ms · Sources: EU EUDAMED, US FDA

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    SARNS

    FDA Adverse Event
    Injury ·3M HEALTH CARE (SARNS)·Product code DWE·January 18, 1995

    TEMPERATURE PROBE CONNECTOR

    FDA Adverse Event
    Injury ·SARNS 3M HEALTH CARE·Product code DWC·March 26, 1997

    MEMBRANE OXYGENATOR

    FDA Adverse Event
    Injury ·SARNS (3M) HEALTH CARE·Product code DTZ·March 19, 1997

    SARNS

    FDA Adverse Event
    SARNS 3M HEALTH CARE·Product code DTZ·August 5, 1995

    TCM II Y CIRCUIT

    FDA Adverse Event
    Malfunction ·SARNS 3M HEALTH CARE, INC.·Product code MJJ·December 6, 1993

    SARNS 9000 5155

    FDA Adverse Event
    Death ·3M HEALTH CARE SARNS PRODUCTS·Product code DTQ·February 9, 1999

    SARNS 1/2" TEMP PROBE CONNECTOR, NON-STERILE BULK PACK

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE. SARNS AND CDI PRODUCTS·Product code DTL·September 19, 1996

    SARNS RIGID ADULT INTRACARDIAC SUCKER

    FDA Adverse Event
    Injury ·3M HEALTH CARE SARNS AND CDI PRODUCTS·Product code DTS·July 31, 1997

    SARNS SOFT FLOW CANNULA

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE SARNS AND CDI PRODUCTS·Product code DWF·July 8, 1997

    OXYGEN-AIR BLENDER

    FDA Adverse Event
    Injury ·3M HEALTH CARE SARNS AND CDI PRODUCTS·Product code JRO·July 31, 1997

    SARNS STERNAL SAW II

    FDA Adverse Event
    Injury ·3M HEALTH CARE SARNS AND CDI PRODUCTS·Product code DWH·April 29, 1997

    SARNS COOLER/HEATER

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE SARNS AND CDI PRODUCTS.·Product code DWC·October 23, 1996

    SARNS STERNAL SAW II

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE, SARN AND CDI PRODUCTS·Product code DWH·October 1, 1996

    SARNS HIGH FLOW AORTIC ARCH CANNULA, 20FR

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE SARNS AND CDI PRODUCTS·Product code DWF·December 12, 1996

    SARNS STERNAL SAW II

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE SARNS AND CDI PRODUCTS·Product code DWH·February 21, 1997

    SARNS STERNAL SAW II

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE, SARNS AND CDI PRODUCTS·Product code DWH·March 20, 1997

    SARNS 7000 MODULAR PUMP, 230 V

    FDA Adverse Event
    Death ·3M HEALTH CARE, SARNS AND CDI PRODUCTS·Product code DWB·March 20, 1997

    SARNS 8000 OCCLUSION SYSTEM

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE SARNS AND CDI PRODUCTS·Product code DTQ·March 10, 1997

    SARNS HIGH FLOW AORTIC ARCH CANNULA

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE SARNS AND CDI PRODUCTS·Product code DQR·March 26, 1997

    SARNS 9000 PERFUSION SYSTEM, 115 V

    FDA Adverse Event
    Other ·3M HEALTH CARE/ SARNS AND CDI PRODUCTS·Product code DTQ·January 12, 1998