IEC 60606 PDF

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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IEC standards Regulation of medical devices. The mandatory date for implementation of the EN European 660606 of the standard is June 1, Take the smart route to ic medical device compliance. Standard Number BS Search all products by. Use British English Oxford spelling from January All articles with unsourced statements Articles with unsourced statements from September Articles with unsourced statements from July Accept and continue Learn more about the cookies we use and how to change your settings.

First published in and regularly updated and restructured, as of it consists of a general standard, about 10 collateral standards, and about 60 particular standards.

BS 5953-1:1980, IEC 60606:1978

The USACanadaJapanAustralia and New Zealand have not yet set transition dates uec their national versions of this latest editionbut the national versions published to date do contain the requirement to also conform with IEC General requirements for basic safety and essential performance – gives general requirements of the series of standards.

Worldwide Standards We iiec source any standard from anywhere in the 606066. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. 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.


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IEC is a series of technical standards for the safety and essential performance of medical electrical equipment, published by the International Electrotechnical Commission. This page was last edited on 9 Novemberat The North American agencies 660606 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.

By using this site, you agree to the Terms of Use and Privacy Policy. August Replaced By: The standard also requires that the manufacturer provide information to the user on how to use the product in the most environmentally sensitive 60066.

BS , IEC – Guide on power transformers. Application of power transformers

We use cookies to make our ieec easier to use and to better understand your needs. 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.


L’application des transformateurs de puissance Title in German Anleitung zu Leistungstransformatoren. Application of power transformers Status: Click to learn more.

From Wikipedia, the free encyclopedia. The faster, easier way to work with standards.

The certification process has been criticized for its complexity, cost, and the business risk it raises. It was the result of a comprehensive review of the second edition dating from Power transformers, Windings, Voltage fluctuations, Temperature rise, Voltage, Electric current, Mathematical calculations, Autotransformers, Magnetic fields, Flux rateThree-phase transformers, Single-phase transformers, Short-circuit currents, Impedance voltage, Electric load, Transformers.

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. This has been more particularly a concern during the transition to the third edition due to the indefinite adoption schedule of the new revision.

Part 1BS Requirements of kec be overridden or bypassed by specific language in the standards for a particular product. Some key changes are: Inthe third edition of IEC was published.

Views Read Edit View history. You may experience issues viewing this site in Internet Explorer 9, 10 or A list of the collateral and particular standards currently in force follows: Your basket is empty. In the United States, nursing facilities are considered to be environments providing professional healthcare.

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