Coagulation Parameters - Models: ACL TOP, ACL TOP CTS, ACL TOP 700, ACL TOP 700 CTS, ACL TOP 700 LAS, ACL TOP 500 CTS, ACL TOP 300 CTS. ANVISA Registry No. 80003610138 의 안전성 경고
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
Access letter NOTIFICATION OF FIELD ACTION. Email: http://portal.anvisa.gov.br/wps/wcm/connect/abdfc98044d9494d871697b0e5034f2e/Carta+Seguran%C3%A7a+Werfen.pdf?MOD=AJPERES
원인
Potential for non-sample identification error in acl top family equipment, occurring only after a specific set of actions combined with the inability of the system to read a bar code from the rack of a specific sample.
조치
Issuance of a letter of safety to distributors and customers with instructions to prevent occurrences of sample identification error. In July / 2015 the company announced the continuation of this field action that corresponds to the importation of software to update the equipment.