OPC Unified Architecture - Part 9: Alarms and Conditions
IEC 62541-9:2020 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition.
IEC 62541-9:2020 specifies the representation of Alarms and Conditions in the OPC Unified Architecture. Included is the…
OPC Unified Architecture - Part 9: Alarms and Conditions
IEC 62541-9:2020 specifies the representation of Alarms and Conditions in the OPC Unified Architecture. Included is the Information Model representation of Alarms and Conditions in the OPC UA address space. Other aspects of alarm systems such as alarm philosophy, life cycle, alarm response times, alarm types and many other details are captured in documents such as IEC 62682 and ISA 18.2. The…
Architecture unifiée OPC - Partie 9: Alarmes et Conditions
L'IEC 62541-9:2020 spécifie la représentation des Alarmes et des Conditions dans l'Architecture unifiée OPC. Il comprend la représentation par le Modèle d'information des Alarmes et des Conditions dans l'espace d'adressage OPC UA. Les autres aspects des systèmes d'alarme tels que la philosophie d'alarme, le cycle de vie, le temps de réponse de l'alarme, les…
Rubber hoses and hose assemblies — Textile-reinforced hydraulic types for oil-based or water-based f...
This document specifies requirements for five types of textile-reinforced hydraulic hoses and hose assemblies of nominal size from 5 to 100.
They are suitable for use with:
— oil-based hydraulic fluids HH, HL, HM, HR and HV as defined in ISO 6743‑4 at temperatures ranging from −40 °C to +100 °C;
— water-based fluids HFC, HFAE, HFAS and HFB as defined in ISO 6743‑4 at temperatures ranging…
Medical devices - Part 1: Application of usability engineering to medical devices
IEC 62366-1:2015+A1:2020 specifies a process for a manufacturer to analyse, specify, develop and evaluate the usability of a medical device as it relates to safety. This usability engineering (human factors engineering) process permits the manufacturer to assess and mitigate risks associated with correct use and use errors, i.e., normal use. It can be used to identify but does not assess or…
Dispositifs médicaux - Partie 1: Application de l'ingénierie de l'aptitude à l'utilis...
L'IEC 62366-1:2015+A1:2020 spécifie un processus permettant à un fabricant d'analyser, de spécifier, de développer et d'évaluer l'aptitude à l'utilisation d'un dispositif médical, concernant la sécurité. Ce processus d'ingénierie de l'aptitude à l'utilisation (ingénierie des facteurs humains) permet au fabricant d'évaluer et de réduire les risques…
