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La présente partie 2-5 de la CEI 61558 est applicable aux blocs d'alimentation pour rasoirs, comprenant un ou plusieurs socles de pr ises de courant et un transformateur de séparation des circuits monophasés à refroidissement...

This part of IEC 60079 specifies requirements for the construction, testing and marking for Group II electrical equipment with type of protection “n” which includes; sealed devices “nC”, hermetically sealed devices “nC”, non...

IEC 60601-2-28:2017 applies to the basic safety and essential performance of X-ray tube assemblies and to components thereof, intended for medical diagnosis and imaging. Where the general standard IEC 60601-1 and the...

1.1 General This standard specifies the requirements for flexible cords, elevator cables, and hoistway cables rated 600 V maximum and electric vehicle cables rated 1000 V maximum and intended for use in accordance with CAN...

This Standard addresses the safe, effective, and reliable reprocessing of reusable medical devices at each phase of the reprocessing workflow and it provides MDR specific requirements for QMS, personnel, MIFUs, purchase and...

ISO 11137-1 describes the requirements for ensuring that the activities associated with the process of radiation sterilization are performed properly. Amendment 2 to included revisions to 4.3.4 and 11.2.

This document provides the requirements and test methods for the safety performance of high pressure gas valves that are used in gaseous hydrogen stations of up to the H70 designation. This document covers the following gas...

This document specifies dimensions and requirements for both open and closed suction catheters made of flexible materials and intended for use in suctioning of the respiratory tract. Suction catheters intended for use with...

This document gives practical guidelines and examples for establishing, implementing, maintaining and improving an energy management system (EnMS) in accordance with the systematic approach of ISO 50001:2018. The guidance in...

The ISO 11138 series provides manufacturers and others with the requirements for production, labeling, test methods and performance requirements of biological indicators used to develop, validate and monitor sterilization...

This document specifies technology that supports the efficient transmission of immersive audio signals and flexible rendering for the playback of immersive audio in a wide variety of listening scenarios. These include home...

This document specifies a set of tests and procedures designed to indicate whether encoders or decoders meet the normative requirements specified in Rec. ITU-T H.265 | ISO/IEC 23008-2. NOTE The conformance bitstreams...