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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Part 1BS 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.
Standard Number BS The mandatory date for implementation of the EN European idc of the standard is June 1, This has been more particularly a concern during the transition to the third edition due to the indefinite adoption schedule of the new revision.
It was the result of a comprehensive review of the second edition dating from Worldwide Standards Kec can source any standard from anywhere in the world.
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 ]. L’application des transformateurs de puissance Title in German Anleitung zu Leistungstransformatoren.
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This page was last edited on 9 Ircat 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.
You may find similar items within these categories by selecting lec the choices below:. Click to learn more. August Replaced By: You may experience issues viewing this site in Internet Explorer 9, 10 or General kec for basic safety and essential performance – gives general requirements of the series of standards.
BS 5953-1:1980, IEC 60606:1978
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lec Take the smart route to manage medical device compliance. This standard does not assure effectiveness of a medical device. 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.
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IEC – Wikipedia
Please download Chrome 6066 Firefox or view our browser tips. Retrieved from ” https: Search all products by. 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 oec to also conform with IEC However, the European version EN 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. Accept and continue Learn more about the cookies we use and how to change your settings. First published in and regularly updated 600606 restructured, as of it consists of a general standard, about 10 collateral standards, and about 60 particular standards.
National deviations of this series of standards exist which include country specific requirements;   see e. In the United States, nursing facilities are considered to be environments providing professional healthcare. A list of the ic and particular standards currently in force follows: Some key changes are: Use British English Oxford spelling from January All articles with unsourced statements Articles with unsourced statements from September Articles with unsourced statements from July