This has been more particularly a concern during the transition to the third edition due to the indefinite adoption schedule of the new revision. Application of power transformers Status: Some key changes are: Standard Number BS
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The USACanadaJapanAustralia and New Zealand have not yet set transition dates for their national versions of this latest editionbut the national versions published to date do contain the requirement to also conform with IEC You may find similar items within uec categories by selecting from the choices below:.
BS , IEC - Guide on power transformers. Application of power transformers
Find Similar Items This product falls into the following categories. This standard does not assure effectiveness of a medical device.
This has been more particularly a concern during the transition to the third edition due to the indefinite adoption schedule of the new revision. Use British English Oxford spelling from January All articles with unsourced statements Articles with oec statements from September Articles with unsourced statements from July IEC must now be incorporated into the design and verification of a wide range of home use and point of care medical devices along with other applicable standards in the IEC 3rd edition series.
This page was last edited on 9 Novemberat BSBS From Wikipedia, the free encyclopedia. Click to 606066 more. National deviations of this series of standards exist which include country specific requirements;   see e.
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Views Read Edit View history. The standard also requires that the manufacturer provide information to the user on how to use the product in the most environmentally sensitive way.
The Part 9 standard asks manufacturers of medical devices to consider the environmental impacts of their devices throughout the product's entire life cycle and to minimize these where possible. The North American agencies will only require these standards for new device submissions, while the EU will take the more severe approach of requiring all applicable devices being placed on the market to consider the home healthcare standard. Particular standards numbered X define the requirements for specific products or specific measurements built into products, e.
You may experience issues viewing 06606 site in Internet Explorer 9, 10 or First published in and regularly updated and restructured, as iiec it consists of a general standard, about 10 collateral standards, and about 60 particular standards.
Take the smart route to manage medical device compliance. Part 1BS Search all products by. Please download Chrome or Firefox or view our browser tips.
BS 5953-1:1980, IEC 60606:1978
General requirements for basic safety and essential performance - gives general requirements of the series 600606 standards.
The mandatory idc for implementation of the EN European version of the standard is June 1, Inthe third edition of IEC was published. Although In Vitro Diagnostic devices such as blood glucose meters are being used by patients at home, the standard does not apply, as these devices remain under the jurisdiction of the more lenient IEC series [ citation needed ].
Collateral standards numbered X define the requirements for certain aspects of safety and performance, e. IEC standards Regulation of medical devices. Learn more about the cookies we use and how to change your settings. IEC is a series of technical standards for the safety and essential performance of medical electrical equipment, published by the International Electrotechnical Commission. Languages Svenska Edit links. Standard Number BS