Information supplied by the manufacturer of medical devicesWhat is this standard about? It exists to help medical device manufacturers comply with the information requirements of the European medical device directives. Who is this standard for? Manufacturers of medical devices Why should you use this standard? It specifies requirements for information to be supplied by manufacturers of medical devices regulated by Council Directive 90 385 EEC relating to active implantable medical devices and Council

BS EN 60974-9 is designed to help with the guidance of instructors

Lift engineers

ISO/IEC 29101 describes a high-level architecture framework and associated controls for the safeguarding of privacy in information and communication technology (ICT) systems that store and process personally identifiable information (PII)

Creation and design of graphical symbols for use in safety signs

BS 6782-1:1987

This standard is not applicable if a large area of the skin (approximately 10% or more of the skin of the whole body) can be in contact with the hot surface

using wrought aluminium alloy

BS 5395-1 on the design of stairs sets out a code of good practice for the design of straight-flight stairs and steps

BS EN 30-1-1 covers the following types of domestic cooking appliances

Method for the determination of pinholes in plastic laminate

the supplier or the distributor to have a quality system in accordance with BS EN ISO 9001 or BS EN ISO 9002

equipment using storage phosphor plates