IS 17724 : Part 4 : 2023 Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use - Part 4 Particular Requirements for In-vitro Diagnostic (IVD) Medical Equipment (IEC 61010-2-101 : 2018, MOD)

ICS 11.040.55; 19.080

MHD 19

NATIONAL FOREWORD

This Indian Standard (Part 4) which is a modified adoption of IEC 61010-2-101 : 2018 'Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment' issued by the International Electrotechnical Commission (IEC) was adopted by Bureau of Indian Standards on the recommendation of Biological Evaluation of Medical Devices and In-vitro Diagnostic 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

.