IEC is a series of technical standards for the safety and essential performance of medical electrical equipment, published by the International. publication, including its validity, is available in the IEC Catalogue of . This first edition of IEC cancels and replaces IEC published in This. IEC , Application guide for power transformers. IEC , Dry- type power transformers. IEC , Guide for the.
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Accept and continue Learn more about the cookies we use and how to change your settings. Requirements of may be overridden or bypassed by specific language in the standards for a particular product.
BS 5953-1:1980, IEC 60606:1978
BS , IEC – Guide on power transformers. Application of power transformers
A list of the collateral and particular standards currently in force follows: List of International Electrotechnical Commission standards. Your basket is empty. Some key changes are: Inthe third edition of IEC was published.
Search all products by. 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. It was the result of a comprehensive review of the second edition dating from Particular standards numbered X define the requirements for specific products or specific measurements built into products, e.
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 IEC standards Regulation of medical devices. Retrieved from ” https: This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.
This standard does not assure effectiveness of a medical device. BSBS 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. The certification process has been criticized for its complexity, cost, and the business risk it raises.
You may experience issues viewing this site in Internet Explorer 9, 10 or 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 ].
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From Wikipedia, the free encyclopedia. The standard also requires that the manufacturer provide information to the user on how to use the product in the most environmentally sensitive way.
Worldwide Standards We can source any standard from anywhere in the world. National deviations of this series of standards exist which include country specific requirements;   see e.