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1.
Zhongguo Yi Liao Qi Xie Za Zhi ; 43(5): 362-364, 2019 Sep 30.
Artigo em Chinês | MEDLINE | ID: mdl-31625337

RESUMO

This article first introduces the regulation requirements for sterilization material in the registration evaluation of sterile medical devices. Secondly, the article chooses the suture passer set kit with multiple sterilization methods as an example product for technical evaluation. The article hopes to provide a reference for the applicant who prepare the registration material and the technical evaluators how to make the evaluation for the medical device registration.


Assuntos
Esterilização , Instrumentos Cirúrgicos
2.
Zhongguo Yi Liao Qi Xie Za Zhi ; 42(5): 375-377, 2018 Sep 30.
Artigo em Chinês | MEDLINE | ID: mdl-30358356

RESUMO

The article collected 250 renew registration of domestic Class Ⅱ passive medical devices from Jan. 2016 to Aug. 2017 in Shanghai. It summarized the common problems listed in the correction notifications of the technical evaluation, and then provides some relevant countermeasures or suggestions. So that we can further speed up the evaluation and approval of medical devices.


Assuntos
Aprovação de Equipamentos , Equipamentos e Provisões , China , Sistema de Registros
3.
Zhongguo Yi Liao Qi Xie Za Zhi ; 41(4): 286-288, 2017 Jul 30.
Artigo em Chinês | MEDLINE | ID: mdl-29862791

RESUMO

This article first introduces the main contents of the requirements for medical device registration. Secondly, this article chooses the vertebral forming surgery system as an example to discuss the technical evaluation for the registration research material. The article hopes to provide a reference for the applicant who prepare the registration material and the technical evaluator who make the evaluation for the medical device registration.


Assuntos
Equipamentos e Provisões , Sistema de Registros , China
4.
Zhongguo Yi Liao Qi Xie Za Zhi ; 37(3): 213-7, 2013 May.
Artigo em Chinês | MEDLINE | ID: mdl-24015619

RESUMO

Recent years, the development of medical devices kits is rapid. How to make the technical evaluation of medical devices kits more perfect bases on the two major principles of safe and effective, and to make kits in the market more normative and orderly, these issues for technical evaluation have to be considered. This article makes a study on current situation of production, classification of management and registration status, combined with existing regulations and related standards, and discusses technical evaluation related issues.


Assuntos
Equipamentos e Provisões/normas
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