DIN EN ISO 5367 [Withdrawn] references following documents:
| Document number | Edition | Title |
|---|---|---|
| EN 556-1 | 2001-10 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices More |
| IEC 60601-1 | 2005-12 | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance More |
| IEC 60417-DB | 2002-10 | Graphical symbols for use on equipment More |
| IEC 60601-1-6 | 2010-01 | Medical electrical equipment - General requirements for basic safety and essential performance - Collateral Standard: Usability More |
| DIN EN ISO 23328-2 | 2009-07 | Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects (ISO 23328-2:2002); German version EN ISO 23328-2:2009 More |
| DIN ISO 7000 | 2008-12 | Graphical symbols for use on equipment - Index and synopsis (ISO 7000:2004 + ISO 7000 Database:2008 up to ISO 7000-2750) More |
| ISO 23328-2 | 2002-10 | Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects More |
| ISO 5362 | 2006-06 | Anaesthetic reservoir bags 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 |
