Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 2: Tests for...
This document specifies tests for the emissions of particulate matter from the gas pathways of a medical device, its parts or accessories, which are intended to provide respiratory care or supply substances via the respiratory tract to a patient in all environments. The tests of this document are intended to quantify particles from 0,25 µm diameter to 10 µm diameter that are emitted by the…
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 1: Evaluatio...
This document specifies:
— the general principles governing the biological evaluation within a risk management process of the gas pathways of a medical device, its parts or accessories, which are intended to provide respiratory care or supply substances via the respiratory tract to a patient in all environments;
— the general categorization of gas pathways based on the nature and duration…
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 4: Tests for...
This document specifies tests for substances leached by liquid water condensing in gas pathways of a medical device, its parts or accessories, which are intended to provide respiratory care or supply substances via the respiratory tract to a patient in all environments. The chemical characterization methods described in this document apply to chemical substances that could leach from the medical…
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 3: Tests for...
This document specifies tests for the emissions of volatile organic substances from the gas pathways of a medical device, its parts or accessories, which are intended to provide respiratory care or supply substances via the respiratory tract to a patient in all environments. The tests of this document are intended to quantify emissions of volatile organic substances that are added to the…
Medical electrical equipment — Part 2-58: Particular requirements for basic safety and essential per...
This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of LENS REMOVAL DEVICES and VITRECTOMY DEVICES for ophthalmic surgery (as defined in 201.3.209 and 201.3.217) and associated ACCESSORIES that can be connected to this MEDICAL ELECTRICAL EQUIPMENT, hereafter referred to as ME EQUIPMENT. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to…
Railway applications — Braking system — General requirements
This document specifies the general requirements for brake systems. This document focuses on general principles and general requirements of brake systems.
This document is applicable for all types of rolling stock during design and whole lifetime. This document does not specify the braking performance criteria.
This document can be applied to all rolling stock with metal to metal wheel/rail…
Évaluation de la biocompatibilité des chemins de gaz respiratoire utilisés dans le domaine de la san...
Le présent document spécifie les essais concernant les émissions de substances organiques volatiles provenant des chemins de gaz utilisés dans un dispositif médical, ses parties ou ses accessoires, qui sont destinés à dispenser des soins respiratoires ou à fournir des substances par les voies respiratoires à un patient dans tous les types d’environnements. Les essais du présent document sont…
Évaluation de la biocompatibilité des chemins de gaz respiratoire utilisés dans le domaine de la san...
Le présent document spécifie les essais concernant les substances relarguées par l’eau liquide qui se condense dans les chemins de gaz utilisés dans un dispositif médical, ses parties ou ses accessoires, destinés à dispenser des soins respiratoires ou à fournir des substances par les voies respiratoires à un patient dans tous les types d’environnements. Les méthodes de caractérisation chimique…
Évaluation de la biocompatibilité des chemins de gaz respiratoire utilisés dans le domaine de la san...
Le présent document spécifie les essais concernant les émissions des matières particulaires provenant des chemins de gaz utilisés dans un dispositif médical, ses parties ou ses accessoires, qui sont destinés à dispenser des soins respiratoires ou à fournir des substances par les voies respiratoires à un patient dans tous les types d’environnements. Les essais contenus dans le présent document…