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| »·¾³ÊÔÑé | GB/T 14710-2009 | Ò½ÓõçÆ÷»·¾³ÒªÇó¼°ÊÔÑéÒªÁì |
| ÐÔÄÜ | EN 13544-1-2007+A1-2009 | Respiratory therapy equipment - Part 1: Nebulizing systems and their components |
| ISO 27427:2023 | Anaesthetic and respiratory equipment Nebulizing systems and components | |
| YY/T 1743-2021 | Âé×íºÍºôÎüÉ豸 Îí»¯ÏµÍ³ºÍ×é¼þ | |
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| ISO 10993-1:2018 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process | |
| ISO 10993-5:2009 | Biological evaluation of medical devices Part 5: Tests for in vitro cytotoxicity | |
| ISO 10993-10:2021 | Biological evaluation of medical devices Part 10: Tests for skin sensitization | |
| ISO 10993-23:2021 | Biological evaluation of medical devices Part 23: Tests for irritation | |
| ISO 18562ϵÁÐ | Biocompatibility evaluation of breathing gas pathways in healthcare applications | |
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