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This part of IEC 60896 applies to all stationary lead-acid cells and monobloc batteries of the valve regulated type for float charge applications, (i.e. permanently connected to a load and to a d.c. power supply), in a static...

This part of IEC 60896 applies to all stationary lead-acid cells and monobloc batteries of the valve regulated type for float charge applications, (i.e. permanently connected to a load and to a d.c. power supply), in a static...

This document specifies requirements for establishing, implementing, maintaining and improving an energy management system (EnMS). The intended outcome is to enable an organization to follow a systematic approach in achieving...

This part of ISO/IEC 9314 specifies a series of tests in order to verify conformance of FDDI stations to the requirements of ISO/IEC 9314-3:1990. NOTE: ISO/IEC 9314-3 specifies the requirements for the optical input/output...

This part of ISO/IEC 13719 defines the binding of the Portable Common Tool Environment (PCTE), as specified in ISO/IEC 13719-1, to the C programming language. A number of features are not completely defined in ISO/IEC 13719-1...

This document specifies the particular requirements, including performance criteria for washer-disinfectors (WD) that are intended to be used for cleaning and chemical disinfection of thermolabile endoscopes. This document...

specifies requirements and provides guidance on the enumeration and microbial characterization of the population of viable microorganisms on or in a health care product, component, raw material or package

specifies general performance requirements for washer-disinfectors (WD) and their accessories that are intended to be used for cleaning and disinfection of re-usable medical devices and other articles used in the context of...

specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices. It also specifies requirements and provides guidance in relation to depyrogenation processes...

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...