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MarED-2014/90/EU船舶MED認證
作者:admin    發布于:2019-02-27 15:10:48    文字:【】【】【

MarED is the co-ordination group for the Notified Bodies assigned by the Member States to carry out the conformity assessment procedures referred to in the Marine Equipment Directive (Directive 2014/90/EU replacing Directive 96/98/EC as amended on Marine Equipment). The MarED Website contains information about the MarED Group, Notified Bodies and the Marine Equipment Directive and equipment certified under the MED (MarED database).

船用設備指令(Marine Equipment Directive - MED)2014/90/EU是歐盟專門為流通于歐洲經濟區內的要裝在船上使用的設備規定的要求,旨在增強海上安全,防止海上污染,并確保這類設備在歐洲共同體內的流通。2014/90/EU指令已取代96/98/EC指令。

根據歐盟認證指令的規定,歐盟相關指令認證只能由歐盟境內注冊的指定機構執行,獲得歐盟授權后,將可以對用于懸掛歐盟船旗船舶的(法定)產品簽發MED認證證書和授予“舵輪”標志。

“舵輪”標志屬于歐盟強制性認證標志,也是歐盟CE認證的一種形式,是歐盟法律對產品提出的一種強制性要求,不論是歐盟內部企業生產的產品,還是其他國家生產的產品,如果要用于懸掛歐盟船旗船舶,就必須獲得指定機構認證并加貼“舵輪”標志,以表明產品符合歐盟船用設備指令(2014/90/EU)的要求。

Context:

Free movement of goods is a cornerstone of the single European market. The European Union has developed original and innovative instruments to remove the barriers to free circulation of goods. The mechanisms in place to achieve this aim are based on prevention of new barriers to trade, mutual recognition and technical harmonisation.

Notified Bodies carry out the tasks pertaining to the conformity assessment procedures referred to in the applicable directives when a third party is required. Member States are responsible for their notification. They may choose the bodies they notify from the bodies under their jurisdiction which comply with the requirements of the directives and the principles laid down in under the EU New Legal Framework (https://ec.europa.eu/growth/single-market/goods/new-legislative-framework_en)

MarED provides a framework for co-ordination and co-operation between its members, the Commission and observers in the application of the Marine Equipment Directive. It is the intention of the MarED to be a conduit for the exchange information between members and to harmonise technical aspects. Furthermore MarED aims at solving unclear situations in reaching a consensus on the procedures of the EC Type Examination and surveillance modules in order to avoid differences between Notified Bodies.

MED認證過程一開始,即對您產品相關的評估程序(模塊)提出建議,然后安全地指引您完成認證過程。這包括您已完成的MED表、所有其它的必要文件以及在經認可的實驗室或驗船師在場時進行的測試。最后,按照歐盟船用產品指令完成產品認證。對于模塊D或E,需要在生產現場進行質量審核。認證過程完成后,立即簽發MED證書。所有的MED認證將列入及MarED-Product(船用設備指令---產品)數據庫中,方便潛在顧客找到您。

通過南京睿督進行MED認證,在所有階段都確保優質服務:
認可過程快捷、高效,省時省錢
專設的MED專家團隊提供指導和支持
有了符合MED所有要求的認證證明,將有機會進入歐洲航運市場

歐盟船用設備指令(MED),為您的船用產品獲得“舵輪標記”認證。

IMO船舶防火測試 http://www.fire-test.com/teststandard/imo/3403.html
船用設備指令(MED)2014/90/EU-船舶IMO MED認證 http://www.fire-test.com/teststandard/imo/12032.html

更多關于MarED及2014/90/EU船舶MED認證相關內容,請咨詢南京睿督公司
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