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.
Panamanian data is current through January 2019. All of the data comes from the Health Ministry (Panama), 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 Panama.
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In panama, the original product, "condones vive original", a contraceptive device, manufactured by thai nippon rubber industry public company limited, thailand, with commercial presentation of white cardboard box in strips x 3 units is registered in panama. the company authorized for marketing has filed complaints that are circulating in stores, supermarkets and other establishments, a condo of doubtful origin, bears the name condones vive original, does not comply with the quality specifications declared in the sanitary registry, the material of packaging is different, the primary or secondary label are different, declares comma manufacturer: karex industries sdn.Bhd. costa rica, and is sold in a transparent plastic bag in long strips of six (6) units, or in a yellow box in strip for six (6); lot l23170806 and expiration date 03/2023.