Medical electrical equipment — Part 2-67: Particular requirements for basic safety and essential per...
This document is applicable to the basic safety and essential performance of oxygen conserving equipment, hereafter referred to as ME equipment, in combination with its accessories intended to conserve supplemental oxygen by delivering gas intermittently and synchronized with the patient's inspiratory cycle, when used in the home healthcare environment. Oxygen conserving equipment is…
Medical electrical equipment — Part 2-69: Particular requirements for the basic safety and essential...
This document specifies requirements for the basic safety and essential performance of an oxygen concentrator in combination with its accessories, hereafter referred to as ME equipment, intended to increase the oxygen concentration of gas intended to be delivered to a single patient. Such oxygen concentrators are typically intended for use in the home healthcare environment by a single patient in…
Medical electrical equipment — Part 2-31: Particular requirements for the basic safety and essential...
IEC 60601-2-31:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of EXTERNAL PACEMAKERS powered by an INTERNAL ELECTRICAL POWER SOURCE, hereafter referred to as ME EQUIPMENT. This document applies to PATIENT CABLES as defined in 201.3.209, but does not apply to LEADS as defined in 201.3.206. HAZARDS inherent in the intended physiological function of ME EQUIPMENT within the scope of this…
Refrigerating systems and heat pumps — Safety and environmental requirements — Part 3: Installation ...
ISO 5149-3:2014 is applicable to the installation site (plant space and services). It specifies requirements for the site for safety, which could be needed because of, but not directly connected with, the refrigerating system and its ancillary components.
ISO 5149-3:2014 is applicable to new refrigerating systems, extensions or modifications of existing systems, and for used systems being…
Piping systems for rehabilitation of underground gas supply networks — Part 1: Polyethylene (PE) mat...
This document specifies requirements and test methods for pipes and fittings which are part of piping systems for the rehabilitation by means of renovation and trenchless replacement of underground gas supply networks.
It is applicable to polyethylene (PE) pipes, fittings and assemblies, as manufactured and as installed. It is not applicable to the existing pipeline.
It is applicable to…
This document specifies requirements and test methods for powered polymerization activators in the 380 nm to 515 nm wavelength region intended for chairside use in polymerization of dental polymer-based materials.
This document applies to quartz-tungsten-halogen lamps and light-emitting diode (LED) lamps. Powered polymerization activators could have internal power supply (rechargeable battery…
Dentistry — Coupling dimensions for handpiece connectors — Part 1: Mechanical properties
This International Standard specifies the coupling between handpieces and motors connected to dental units.
This International Standard specifies the nominal dimensions, tolerances and the extraction force of coupling systems for use between handpiece and motor which supply the handpiece with water, air and light, and rotation energy.
Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum
ISO 7396-1:2016 specifies requirements for design, installation, function, performance, testing, commissioning and documentation of pipeline systems used in healthcare facilities for the following:
- oxygen;
- nitrous oxide;
- medical air;
- carbon dioxide;
- oxygen/nitrous oxide mixtures (see Note 1);
- helium/oxygen mixtures;
- (*) oxygen 93;
- gases and gas mixtures classified as medical…
Steel structures — Structural bolting — Test method for determining the slip factor for faying surfa...
The standard is to provide a test method and associated criteria to determine the slip factor for a particular faying surface treatment, with or without a faying surface coating.