Search

This part of ISO/IEC 24791 defines an interface within the Software System Infrastructure (SSI) that provides RFID system control components with low-level access to RFID interrogators for the purpose of optimizing RFID data...

ISO 10524-1:2018 specifies the design, construction, type testing, and marking requirements for pressure regulators intended for the administration of medical gases and their mixtures in the treatment, management, diagnostic...

ISO 10524-2:2018 specifies design, construction, type testing, and marking requirements for manifold pressure regulators and line pressure regulators intended for use in medical gas pipeline systems. Examples of gases include...

This document specifies design, type testing, and marking requirements for cylinder valves with integrated pressure regulators [as defined in 3.26 and referred to hereafter as valves with integrated pressure regulators (VIPRs...

ISO 9170-1:2017 is intended especially to ensure the gas-specific assembly, mechanical resistance, flow, leakage and pressure drop of terminal units and to prevent their interchange between different gases and services and...

This part of ISO/IEC 14496 specifies the ISO base media file format, which is a general format forming the basis for a number of other more specific file formats. This format contains the timing, structure, and media...

This part of ISO/IEC 30134 specifies the following for the other parts of ISO/IEC 30134: a) a common structure; b) definitions, terminology and boundary conditions for KPIs of data centre resource usage effectiveness and...

This part of ISO/IEC 30134 specifies the power usage effectiveness (PUE) as a key performance indicator (KPI) to quantify the efficient use of energy in the form of electricity. This part of ISO/IEC 30134 a) defines the power...

This part of ISO/IEC 30134 a) defines the renewable energy factor (REF) of a data centre b) specifies a methodology to calculate and to present the REF, and c) provides information on the correct interpretation of the REF.

ISO 10079-2:2014 specifies safety and performance requirements for medical, manually powered suction equipment intended for oro-pharyngeal suction. It covers equipment operated by foot or by hand or both. Annex C illustrates...

ISO 10079-3:2014 specifies safety and performance requirements for medical suction equipment powered from a vacuum or positive pressure gas source generating venturi suction. It applies to equipment connected to medical gas...

ISO 23328-1:2003 gives a short-term airborne sodium chloride particle challenge test method for assessing the filtration performance of breathing system filters (BSF) intended for the filtration of respired gases