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.
Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
데이터 추가 비고
The cited problem can occur every time the following events occur simultaneously: a patient is selected in the patient list, the examination tab is pressed and a query to the database is running at the same time in the background. According to Philips Medical System Ltda (holder of product registration in Brazil), the equipment will be updated with a software version that will correct this error. The company has not yet released the timeline for correcting the error. The ANVISA Technovigilance Unit is monitoring this case.
원인
The equipment may perform an incorrect selection of patients, which may cause confusion of data belonging to different patients.
조치
The recommended action for product users is that, before saving the images, check the patient selection list if the correct patient is selected.