NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 80601-2-79 [Pre-order] references following documents:
| Document number | Edition | Title |
|---|---|---|
| ISO 7396-1 AMD 1 | 2017-12 | Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum; Amendment 1 More |
| ISO 80601-2-74 | 2021-07 | Medical electrical equipment - Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment More |
| ISO 9360-1 | 2000-03 | Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml More |
| ISO 9360-2 | 2001-04 | Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml More |
| ISO 80369-1 | 2018-11 | Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements More |
| DIN EN ISO 10524-1 | 2024-01 | Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (ISO 10524-1:2018 + Amd 1:2023); German version EN ISO 10524-1:2019 + A1:2023 More |
| DIN EN ISO 14159 | 2008-07 | Safety of machinery - Hygiene requirements for the design of machinery (ISO 14159:2002); German version EN ISO 14159:2008 More |
| DIN EN ISO 14937 | 2010-03 | Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009); German version EN ISO 14937:2009 More |
| DIN EN ISO 15223-1 | 2022-02 | Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021); German version EN ISO 15223-1:2021, with CD-ROM More |
| DIN EN ISO 17664-1 | 2021-11 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021); German version EN ISO 17664-1:2021 More |
