[How to apply for european CE certification for Chinese medical device manufacturers]

Full Abstract

The paper introduces the requirements of European medical device regulation and tells Chinese medical device manufacturers how to comply with this regulation.

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Author information

Author/s: Xu, Xing-gang (XG);

Affiliation: Medical-Health-Service Dept, Jiangsu TUV Product Service Ltd., Shanghai Branch.

Journal and publication information

Publication Type: English Abstract; Journal Article

Journal: Zhongguo yi liao qi xie za zhi = Chinese journal of medical instrumentation (Zhongguo Yi Liao Qi Xie Za Zhi), published in China. (Language: chi)

Reference: 2006-Nov; vol 30 (issue 6) : pp 453-6

Dates: Created 2007/02/15; Completed 2007/12/27;

PMID: 17300018, status: MEDLINE (last retrieval date: 12/26/2008)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

China
Device Approval - standards
Equipment Safety

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