BEUDAMED
    262 results · 105ms · Sources: EU EUDAMED, US FDA

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    Body Supports and Belts

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·AADHAR MEDICARE PRIVATE LIMITED·71 devices

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·October 2, 2007

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORP·Product code MVK·November 9, 2009

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 5, 2009

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 31, 2009

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·March 6, 2008

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code ---·March 11, 2008

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 7, 2008

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 14, 2008

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 20, 2009

    FLAMINGO

    FDA Adverse Event
    Injury ·R82 A/S·Product code INM·March 22, 2021

    RoboCouch Patient Support System, a component of the CyberKnife Robotic Radiosurgery System. Model number 025007, manufactured by Accuray Inc., Sunnyvale, CA The CyberKnife is indicated for treatment planning and imageguided stereotactic radiosurgery and precision radiotherapy of lesions, tumors and conditions anywhere in the body when radiation treatment is indicated. The RoboCouch Patient Support System is intended for use in the support and positioning of a patient during Radiosurgery and radiotherapy procedures and other medical procedures when precise positioning is required.

    FDA Recall
    Terminated ·Accuray Inc·Product code JAI·October 30, 2008

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 19, 2009

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 7, 2008

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 9, 2011

    ENCORE

    FDA Adverse Event
    Malfunction ·ARJO MED. AB LTD.·Product code FSA·April 9, 2019

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORP·Product code MVK·March 9, 2011

    PROFEX

    FDA Adverse Event
    Injury ·PROFEX MEDICAL PRODUCTS·Product code FMQ·May 31, 2007

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Death ·ZOLL LIFECOR CORPORATION·Product code MVK·March 3, 2008

    SLINGS, CLIP

    FDA Adverse Event
    Malfunction ·ARJO DOMINICAN REPUBLIC·Product code FSA·July 25, 2023