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.
Colombian data is current through June 2019. All of the data comes from the National Institute of Drugs and Food Surveillance (INVIMA), 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 recall data from the U.S. and Colombia.
데이터 추가 비고
원인
The manufacturer reports that they have detected incidents with the medical devices referenced when the central axis is released, originated by an error in the assembly of the safety rings of the support arm, leading to the presence of potential adverse events on the patients or users.
TruLight 3000, TruLight 5000, iLed 3, iLed 5 and TruVidia
제품 설명
This device is used to illuminate a zone of the patient who was examining or operating in hospitals or medical consultations locally with a high luminous intensity.