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

This has been more particularly a concern during 60660 transition to the third edition due to the indefinite adoption schedule of the new revision. You may find similar items within these categories by selecting from the choices below:.

August Replaced By: It was the result of a comprehensive review of the second edition dating from 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 Click to learn more.

This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. National deviations of this kec of standards exist which include country specific requirements; [3] [4] see e. IEC standards Regulation of medical devices.

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We use cookies to make our website easier to use and to better understand your needs. Languages Svenska Edit links. This page was last edited on 9 Novemberat Some key changes are: Your basket is empty. In the United States, nursing facilities are considered to be environments providing professional healthcare.

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Take the smart route to manage medical device compliance. Collateral standards numbered X define the requirements for certain aspects of safety and oec, e. Inthe third edition of IEC was published. General requirements for basic safety and essential performance – gives general requirements of the series of standards.

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. Part 1BS By using this site, you agree to the Terms of 06606 and Privacy Policy. The certification process has been criticized for its complexity, cost, and the business risk it raises.

The standard also requires that the manufacturer provide information to the user on how to use the product in the most environmentally sensitive way. Learn more about the cookies we use and how to change your settings.

L’application des transformateurs de puissance Title in German Anleitung zu Leistungstransformatoren. Views Read Edit View history.

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The mandatory date for implementation of the EN European version of the standard is June 1, 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. Please download Chrome or Firefox or view our browser tips.

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A list of the collateral and particular standards currently in force follows: 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.

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 ].

BS 5953-1:1980, IEC 60606:1978

IEC is a series of technical standards for the safety and essential performance of medical electrical equipment, published by the International Electrotechnical Commission. Accept and continue Learn more about the cookies we use and how to change your settings. Worldwide Standards We can source any standard from anywhere in the world.

Standard Number BS

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