prBAS EN IEC 61557-16:2025
Electrical safety in low voltage distribution systems up to 1 000 V AC and 1 500 V DC - Equipment for testing, measuring or monitoring of protective measures - Part 16: Equipment for testing the effectiveness of the protective measures of electrical equipment and/or medical electrical equipment
General information
Status:Project
Number of pages:42
Adoption method:Proglašavanje
Language:engleski
Edition:1.
Realization date:04.12.2024
Forseen date for next stage code:17.12.2024
Technical committee:BAS/TC 10, Electrical energy measurement equipment and load control
Directives:
2014/35/EU, Directive 2014/35/EU of the European Parliament and of the Council of 26 February 2014 on the harmonisation of the laws of the Member States relating to the making available on the market of electrical equipment designed for use within certain voltage limits
2014/30/EU, Directive 2014/30/EU of the European Parliament and of the Council of 26 February 2014 on the harmonisation of the laws of the Member States relating to electromagnetic compatibility (recast)
2014/30/EU, Directive 2014/30/EU of the European Parliament and of the Council of 26 February 2014 on the harmonisation of the laws of the Member States relating to electromagnetic compatibility (recast)
ICS:
29.080.01, Electrical insulation in general
17.220.20, Measurement of electrical and magnetic quantities
17.220.20, Measurement of electrical and magnetic quantities
Abstract
IEC 61557-16:2023 specifies the requirements applicable to the performance for test and measurement equipment in order to determine the effectiveness of the protective measures for electrical equipment and/or medical electrical equipment described in IEC 62353.
This International Standard is to be used in conjunction with IEC 61557-1:2019.
IEC 61557-16:2023 cancels and replaces the first edition published in 2014. This edition constitutes a technical revision.
This edition includes the following significant technical changes with respect to the previous edition:
a) splitting of uncertainty requirements for medical and non-medical electrical equipment in 4.2.1;
b) addition of a definition of ranges with defined uncertainty in 4.2.1 to 4.2.7;
c) addition of an optional measuring device (MD) for non-medical devices in 4.2.1;
d) addition of a limitation of the maximum intrinsic uncertainty for medical applications at leakage current in 4.2.1;
e) change of 4.2.3 from test sockets to sockets for service purposes;
f) addition of a warning in the operating instructions;
g) integration of former 6.3 into 6.2;
h) update of Table 1;
i) alignment of the structure with that of the whole IEC 61557 series.
Lifecycle
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Original document and degree of correspondence
EN IEC 61557-16:2024, identical
IEC 61557-16:2023, identical
Relation to BAS standards
Work material
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