BEUDAMED
    68 results · 86ms · Sources: EU EUDAMED, US FDA

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    SERVO VENTILATOR

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SYSTEMS,INC. ELECTROMEDICAL GROUP·Product code CBK·August 12, 1996

    SIEMENS MEDICAL SYSTEMS VENTILATOR

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL GRP.·Product code CBK·August 12, 1996

    SIEMENS

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL DIVISION·Product code CBK·May 19, 2000

    SIEMENS

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL DIV.·Product code DRT·November 8, 2000

    SERVO MECHANICAL VENTILATOR

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL GRP.·Product code CBK·April 15, 1997

    TELEMETRY MONITORING SYSTEM

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL GRP·Product code DRG·November 18, 1996

    SIEMENS

    FDA Adverse Event
    SIEMENS MEDICAL SYSTEMS INC. ELECTROMEDICAL DIV.·Product code MHX·December 7, 2000

    SIEMANS SERVO 900C

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL DIV.·Product code CBK·September 13, 1999

    SIEMENS SERVO 900C

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL DIV.·Product code CBK·September 13, 1999

    SIEMANS SERVO 900C

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL DIV.·Product code CBK·September 13, 1999

    SERVO VENTILATOR 900C

    FDA Adverse Event
    Death ·SIEMENS MEDICAL SYSTEMS, INC/ELECTROMEDICAL GROUP·Product code CBK·January 22, 1998

    SIEMENS

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS INC. ELECTROMEDICAL DIVISION·Product code CBK·December 22, 1998

    SERVO VENTILATOR

    FDA Adverse Event
    Death ·ELECTROMEDICAL GROUP SIEMENS MEDICAL SYSTEMS, INC.·Product code CBK·January 30, 1996

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·June 1, 2022

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·April 11, 2024

    RITA StarBurst (2-3cm Diameter/25cm Length), Electro-surgical Device, Manufactured by: RITA Medical Systems, Inc., One Horizon Way, Manchester, GA 31816

    FDA Recall
    Terminated ·Rita Medical Systems, Inc.·Product code GEI·April 3, 2007

    SIEMENS-ELEMA VENTILATOR

    FDA Adverse Event
    Injury ·ELECTRO MEDICAL GROUP SIEMENS MEDICAL SYSTEMS, INC.·Product code CBK·June 28, 1996

    SIEMENS MEDICAL SYSTEMS INC.

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SYSTEMS INC. ELECTROMEDICAL SYSTEMS DIVISION·Product code CBK·January 6, 2003

    SIEMENS

    FDA Adverse Event
    Death ·SIEMENS MEDICAL SYSTEMS, INC. ELECTRO MEDICAL DIVISON·Product code DRT·September 29, 1998

    SIEMENS

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL SYSTEMS DIV.·Product code CBK·November 26, 2002