Application name: Applicator for laser surgery Technical Name: Applicators Registration Number ANVISA: 80058580020 Hazard Class: III Model Affected: CR-XXX, CA-XX-YYY, CB-XXX-YYY Serial Numbers Affected: laser model CA-30-250 with aspiration - Code 015093 - Lot 16 I 003 Applicator for laser surgery model CA-30-250 without aspiration - Code 015071 - Lot 16 I 002 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Vydence Medical - Indústria e Comércio Ltda.; Vydence Medical - Indústria e Comércio Ltda. 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
  • 사례 ID
    2185
  • 날짜
    2017-02-10
  • 사례 국가
  • 사례 출처
    ANVISA
  • 사례 출처 URL
  • 비고 / 경고
    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
    Guidelines for regulated entities at any level: • Segregate and discontinue use of models and batches of products under this recall. • Check your inventory to determine if you own any of the products listed above. • If you have already sold some or all of the products, contact your customer and require their traceability for the affected products. It is reinforced that the return and full communication of traceability of the requested products is obligatory, according to the bond of joint responsibility, which is formed when the products are supplied to customers. To return the products, please call the Customer Service at (0xx16) 3306-5050, to inform the details of the product that will be returned.
  • 원인
    We received a technical complaint from a company customer on 11/01/2017, pointing out a suspicious-looking product in your inventory. this product presented a label that the customer described as "strange." when we received more details via email we noticed that the label used was not the one recommended in the product registration.
  • 조치
    Field Action Code Notification 2017.02.001370 triggered under the responsibility of the company Vydence Medical - Indústria e Comércio Ltda. Company will collect.