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欧盟在内窥镜检查方面的新规定。

New EU regulations in endoscopy.

作者信息

Wächter M, Diekjobst T

机构信息

Olympus Optical Company, Hamburg, Germany.

出版信息

Endoscopy. 1995 Sep;27(7):512-5. doi: 10.1055/s-2007-1005758.

Abstract

As a result of European unification, new regulations valid within the territory of the European Union (EU) have been negotiated and published. As in other medical fields, the Medical Device Directive (MDD) is the most important new regulation and also effects endoscopy. In a transition period until June 1998, the MDD will be transposed into national law by the member states of the EU. Compliance with the MDD and other European regulations is indicated by the CE mark affixed to the product.

摘要

由于欧洲一体化,在欧盟(EU)境内有效的新法规已经协商并发布。与其他医学领域一样,《医疗器械指令》(MDD)是最重要的新法规,也对内镜检查产生影响。在1998年6月之前的过渡期内,欧盟成员国将把MDD转化为本国法。产品贴上CE标志表明符合MDD及其他欧洲法规。

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