IS 17784 : Part 2 : 2023 Electrical Equipment for Measurement, Control and Laboratory Use - EMC Requirements Part 2 Particular Requirements for In-vitro Diagnostic (IVD) Medical Equipment (IEC 61326-2-6 : 2020, MOD)

NATIONAL FOREWORD

This Indian Standard (Part 2) is a modified adoption of IEC 61326-2-6 : 2020 'Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2: Particular requirements - Section 6: Particular requirements - In-vitro diagnostic (IVD) medical equipment' issued by the International Electrotechnical Commission (IEC) was adopted by Bureau of Indian Standards on the recommendation of in-vitro Diagnostic Medical Devices and Biological Evaluation of Medical Devices Sectional Committee and approval of the Medical Equipment and Hospital Planning Division Council.

The text of IEC standard has been approved as suitable for publication as an Indian Standard without deviations. Certain conventions and terminologies are, however, not identical to those used in Indian Standards. Attention is particularly drawn to the following:

 a) Wherever the words 'International Standard' appear referring to this standard, they should be read as 'Indian Standard'; and

 b) Comma (,) has been used as a decimal marker while in Indian Standards, the current practice is to use a point (.) as the decimal marker.