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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You may find similar items within these categories by selecting from idc choices below:. National deviations of this series of standards exist which include country specific requirements; [3] [4] see e. Part 1BS BSBS You may experience issues viewing this site in Internet Explorer 9, 10 or Search all products by.

In the United States, nursing facilities are considered to 6606 environments providing professional healthcare. 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 Inthe third edition of IEC was published.

A list of the collateral and particular standards currently in force follows: IEC is a series of technical standards for the safety and essential performance of lec electrical equipment, published by the International Electrotechnical Commission. This standard does not assure effectiveness of a medical device.

Find Similar Items This product falls into the following categories. 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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The mandatory date for implementation of the EN European version of the standard is June 1, This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Use British English Oxford spelling from January All articles with unsourced statements Articles with unsourced statements from September Articles with unsourced statements from July First published in and regularly updated and restructured, as of it consists of a general standard, about 10 collateral iecc, and about 60 particular standards.

This has been more particularly a concern during the transition to the third edition due to the indefinite adoption schedule of the new revision. Power transformers, Windings, Voltage fluctuations, Temperature rise, Voltage, Electric current, Mathematical calculations, Autotransformers, Magnetic fields, Flux rateThree-phase transformers, 60660 transformers, Short-circuit currents, Impedance voltage, Electric load, Transformers.

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BS 5953-1:1980, IEC 60606:1978

Requirements of may be overridden or bypassed by specific language in the standards for a particular product. Click ied learn more. By using this site, you agree to the Terms of Use and Privacy Policy.

Learn more about the cookies we use and how to change your settings. General requirements for basic safety and essential performance – gives general requirements of the series of standards. Although In Vitro Diagnostic 6006 such as blood glucose meters are 606006 used by patients at home, the standard does not apply, as these devices remain under the jurisdiction of the more lenient IEC series [ iev needed ].

L’application des transformateurs de puissance Title in German Anleitung zu Leistungstransformatoren. Languages Svenska Edit links.

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.

Some key changes are: August Replaced By: It was the result of a comprehensive review of the second edition dating from This page was last edited on 9 Novemberat List of International Electrotechnical Commission standards.

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The faster, easier way to work with standards. The certification process has been criticized for its complexity, cost, and the business risk it raises.

IEC – Wikipedia

Application of power transformers Status: 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.

IEC standards Regulation of medical devices. Take the smart route to manage medical device compliance. Views Read Edit View history. Your basket is empty. Particular standards numbered X define the requirements for specific products or specific measurements built into products, e. Standard Number BS Accept and continue Learn more about the cookies we use and how to change your settings. We use cookies to make our website easier to use and to better understand your needs.

Collateral standards numbered X define the requirements for certain aspects of safety and performance, e. However, the European version EN From Wikipedia, the free encyclopedia. Retrieved from ” https: Worldwide Standards We can source any standard from anywhere in the world.

The standard also requires that the manufacturer provide information to the user on how to use the product in the most environmentally sensitive way. Please download Chrome or Firefox or view our browser tips.