En 62479 en 62311 pdf

The objective is to determine the compliance of eut with en 62479. Assessment of electronic and electrical equipment related to. For convenience of the reader, in the remainder of this ecma tr reference will be made to both standards as follows. The objective is to determine the compliance of eut with en 50663. The equivalent european standard, en 62311 2 followed in 2008. For more details, see table and calculations below.

Secure pdf files include digital rights management drm software. May 2008 assessment of electronic and electrical equipment related to human exposure. Iec 62311 defines measurement procedures, not limit values. Ecma tr97 guide for assessment of human exposure to. For the purposes of the assessment detailed in this test report the basic standard en 50383 was used. This product has been tested and found to comply with the electromagnetic compatibility emc limits for a class b digital device pursuant to the listed directives, regulations and standards.

Assessment of the compliance of low power electronic and electrical equipment with the basic restrictions related to human exposure to electromagnetic fields 10 mhz to 300 ghz. Product specifications for the hp envy 5052 allinone. Din en 62479 201109 assessment of the compliance of low power electronic and electrical equipment with the basic restrictions related to human exposure to electromagnetic fields 10 mhz to 300 ghz iec 62479. Assessments should be made in accordance with an existing basic standard. Publisher european committee for standards electrical. Emf assessment, then other standards, including iec 62311 or other emf product. Radio frequency exposure test report en 62311 january. En 62311 assessment methods en 62311 allows for various assessment methods, including far field calculation, near field calculation, simulation, and numerical modeling. It is harmonized with the international iec standard and is already incorporated into national standards the next lower level. All bsi british standards available online in electronic and print formats. Safety distance of antenna depending on antenna gain d db i antenna gain r.

The standard in the uk, for example, is bs en 62311 3. Emf test report for intel corporation intel nuc model name. Notified bodies for directive 201435eu of the ep and of the council. The object of this standard is to demonstrate the compliance of such apparatus with the basic. Declaration of conformity according to isoiec 170501 and en 170501. Or download the pdf of the directive or of the official journal for free this website uses cookies to ensure you get the best experience on our website. Assessment of the compliance of low power electronic and.

The standard iecen 62311 is a generic standard that is applicable for all electrical and electronic equipment. The standard iec en 62311 is a generic standard that is applicable for all electrical and electronic equipment. The text of document 106198fdis, future edition 1 of iec 62479, prepared. This tr provides guidance on the application of iecen 62311 with practical. Declaration of conformity according to isoiec 17050. Or download the pdf of the directive or of the official journal for free. New standard on human exposure to em fields interference. Other similar equipment will not nece ssarily produce the same results. May 2008 assessment of electronic and electrical equipment related to human exposure restrictions for electromagnetic fields 0 hz 300 ghz. Radio frequency exposure test report en 62311 january 2008.

Worldwide regulatory compliance engineering and environmental. Emf assessment, then other standards, including iec 62311 or other emf product standards, may be used for conformity assessment. Test methodology all measurements contained in this report were conducted with en 62479. According to en 62311 the following maximum power densities s eq are defined. Emf test report for intel corporation intel nuc model. En 62479 annex10 mhz b radio transmitter communication300 ghz fixed, mobile or portable use. Declaration of conformity according to isoiec 170501 and en. En 50371 or is medical equipment as defined in the council directive 9342eec of 14 june 1993 concerning medical devices. The results of testing in this report apply only to the productsystem, which was tested.