Monitor/ Defibrillator DEFIGARD Touch7 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Schiller Medical 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2018-01-30
  • 사례 출판 날짜
    2017-01-30
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: schiller medical, monitor/ defibrillator defigard touch7 the health sciences authority (hsa), singapore posted a medical device safety alert concerning monitor/ defibrillator defigard touch7 [all devices with software version up to “soft 5” are affected]. the defigard touch7 can be configured in 3 different start modes (monitoring, aed or manual defibrillator). the field safety notice concerns devices configured in start mode “manual defibrillator’. if the user starts the device in this configuration, and switches directly from the manual defibrillation to the synchronized defibrillation mode, without ecg patient cable being plugged, then the device will be unable to trigger the synchronized defibrillation shock. this can be seen on the screen of the device, no trigger pulses are available. if the patient cable is connected, according to the user manual, this failure does not occur. according to the manufacturer, it may be unable to perform synchronized defibrillation therapy. the manual defibrillation mode at start is a specific medical emergency service setting. it is used when rescuer wants to mainly use the device as manual defibrillator. the synchronized defibrillation is not an emergency procedure, and it is recommended to perform it with ecg patient cable. while waiting for the update of the defigard touch 7, affected users are advised to continue to use it without restriction. if user startup configuration with manual defibrillation mode, user has to select another startup mode, until the update to software “soft 6”, or use a patient cable for the synchronized defibrillation therapy, as described in the user manual. for details, please visit the following hsa website: http://www.Hsa.Gov.Sg/content/dam/hsa/hprg/medical_devices/updates_and_safety_reporting/field_safety_corrective_action/fsn/2017/november/hsa%206004101-056-17-06_36%20fsn_redacted.Pdf if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 30 january 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Schiller Medical, Monitor/ Defibrillator DEFIGARD Touch7
  • Manufacturer

Manufacturer