Cryogenic vessels — Pressure-relief accessories for cryogenic service — Part 3: Sizing and capacity ...
ISO 21013-3:2016 provides separate calculation methods for determining the required mass flow to be relieved for each of the following specified conditions:
- vacuum-insulated vessels with insulation system (outer jacket + insulating material) intact under normal vacuum, outer jacket at ambient temperature, inner vessel at temperature of the contents at the specified relieving pressure;
- vacuum-…
Geometrical product specifications (GPS) — Acceptance and reverification tests for coordinate measur...
This document defines the language of symbols used in the ISO 10360 series of documents to identify metrological characteristics of coordinate measuring systems (CMSs) and their maximum permissible errors (MPEs) or limits (MPLs).
Information technology — Portable Operating System Interface (POSIX®) base specifications — Issue 8
ISO/IEC/IEEE 9945:2009 defines a standard operating system interface and environment, including a command interpreter (or "shell"), and common utility programs to support applications portability at the source code level. ISO/IEC/IEEE 9945:2009 is intended to be used by both application developers and system implementers and comprises four major components (each in an associated volume…
Information technology — Radio frequency identification device conformance test methods — Part 6: Te...
ISO/IEC 18047-6 defines test methods for determining the conformance of radio frequency identification (RFID) devices (tags and interrogators) for item management with the specifications given in ISO/IEC 18000-61, ISO/IEC 18000-62, ISO/IEC 18000-63 and ISO/IEC 18000-64, but does not apply to the testing of conformity with regulatory or similar requirements.
The test methods require only that the…
Ergonomie des ambiances thermiques — Évaluation des ambiances thermiques dans les véhicules — Partie...
L'ISO 14505-2:2006 donne des lignes directrices relatives à l'évaluation des conditions thermiques à l'intérieur d'un habitacle de véhicule. Elle peut également s'appliquer à d'autres espaces confinés où règnent des conditions climatiques asymétriques. Elle est essentiellement destinée à l'évaluation des conditions thermiques, lorsque les écarts par rapport à la…
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…
Irrigation techniques — Remote monitoring and control for irrigation systems — Part 1: General consi...
The scope of this NWIP is to develop standards related to the remote monitoring and control for irrigation systems, using different technologies.
This part of the standard is intended to define the general considerations applicable to all kind of RMCS used in irrigation.
Additionally, the document includes some specific clauses intended to any RMCS that includes, totally or partially,…
Extracorporeal systems for blood purification — Part 2: Extracorporeal blood and fluid circuits for ...
This document specifies requirements for disposable extracorporeal blood and fluid circuits and accessories used in combination with haemodialysis equipment intended for extracorporeal blood treatment therapies such as, but not limited to, haemodialysis, haemodiafiltration, haemofiltration.
This document does not apply to:
— haemodialysers, haemodiafilters or haemofilters;
— plasmafilters…
Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilter...
This document specifies requirements and test methods for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators, hereinafter collectively referred to as “the device”, for use in humans.
This document does not apply to:
— extracorporeal blood circuits;
— plasmafilters;
— haemoperfusion devices;
— vascular access devices;
— blood pumps;
— systems to prepare,…
Extracorporeal systems for blood purification — Part 3: Plasmafilters
This document specifies requirements and test methods for plasmafilters, which are devices intended to separate plasma from blood in therapeutic plasmapheresis therapy. This document specifies the requirements for sterile, single-use plasmafilters, intended for use on humans, hereinafter collectively referred to as “the device”, for use in humans. This document does not apply to;
— …