Medical electrical equipment. General requirements for safety - Collateral standard. General requirements for programmable electrical medical systemsMedical electrical equipment Part 1 4: General requirements for safety Collateral standard: Programmable electrical medical systems Executive summary General requirements for safety and design of programmable electrical medical systems. Abstract This European Standard specifies requirements for the process by which a programmable electrical medical systems (PEMS) is designed. This Standard also serves as the basis for requirements of Particular

The range of 600/1 000 V cables has been widened by adding 400 mm2 sizes for four-core cables

S355G10+N - up to and including 150 mm

normal hexagonal head

Beams which are part of a floor construction are tested with the floor construction as described in EN 1365-2 and are subject to evaluation of integrity and insulation

Compliance with BS EN 473:2008 provides proof of NDT expertise

These criteria and limits are primarily intended to guide the design of new or refurbished buildings undergoing a change of use

This European Standard includes the following cross-references:

In all other respects such lifts are designed in accordance with BS EN 81–1

and includes those that may have particular meanings when used in different areas of industry and commerce

This standard defines a biometric data block format that contains a digital record of the image of a face

quality and strength of personal fall protection equipment and enhancing safety

military establishments