NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 5361 [Withdrawn] references following documents:
Document number | Edition | Title |
---|---|---|
DIN EN ISO 18562-1 | 2020-05 | Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1: Evaluation and testing within a risk management process (ISO 18562-1:2017); German version EN ISO 18562-1:2020 More |
DIN EN ISO 18562-2 | 2020-05 | Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 2: Tests for emissions of particulate matter (ISO 18562-2:2017); German version EN ISO 18562-2:2020 More |
DIN EN ISO 18562-3 | 2020-05 | Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 3: Tests for emissions of volatile organic compounds (VOCs) (ISO 18562-3:2017); German version EN ISO 18562-3:2020 More |
DIN EN ISO 18562-4 | 2020-05 | Biocompatibility evaluation of breathing gas pathways in healthcare application - Part 4: Tests for leachables in condensate (ISO 18562-4:2017); German version EN ISO 18562-4:2020 More |
DIN EN ISO 4135 | 2022-06 | Anaesthetic and respiratory equipment - Vocabulary (ISO 4135:2022); Trilingual version EN ISO 4135:2022 More |
DIN EN ISO 5356-1 | 2015-06 | Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets (ISO 5356-1:2015); German version EN ISO 5356-1:2015 More |
DIN EN ISO 5366 | 2017-04 | Anaesthetic and respiratory equipment - Tracheostomy tubes and connectors (ISO 5366:2016); German version EN ISO 5366:2016 More |
DIN EN ISO 80369-7 | 2021-08 | Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2021); German version EN ISO 80369-7:2021 More |
DIN EN ISO 80601-2-12 ; VDE 0750-2-12:2020-07 | 2020-07 | Medical electrical equipment - Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators (ISO 80601-2-12:2020); German version EN ISO 80601-2-12:2020 More |
ISO 10993-1 | 2018-08 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process More |