NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 11737-2 [Withdrawn] referenced in following documents:
| Document number | Edition | Title |
|---|---|---|
| DIN 58921 | 2011-01 | Test method to demonstrate the suitability of a medical device simulator during steam sterilisation - Medical device simulator testing; Text in German and English More |
| VDI 5701 | 2018-05 | Biomaterials in medicine - Classification, requirements, and applications More |
| VDI 2083 Blatt 21 | 2019-10 | Cleanroom technology - Cleanliness of medical devices in the manufacturing process More |
| DIN EN ISO 11138-7 | 2019-11 | Sterilization of health care products - Biological indicators - Part 7: Guidance for the selection, use and interpretation of results (ISO 11138-7:2019); German version EN ISO 11138-7:2019 More |
| DIN EN ISO 13408-7 | 2015-11 | Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012); German version EN ISO 13408-7:2015 More |
| DIN EN ISO 14534 | 2015-08 | Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements (ISO 14534:2011); German version EN ISO 14534:2015 More |
| DIN EN ISO 15883-1 | 2014-10 | Washer-disinfectors - Part 1: General requirements, terms and definitions and tests (ISO 15883-1:2006 + Amd 1:2014); German version EN ISO 15883-1:2009 + A1:2014 More |
| DIN EN ISO 20857 | 2013-08 | Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010); German version EN ISO 20857:2013 More |
| KHHygieneAnfMedPEmpf | 2012-10 | Anforderungen an die Hygiene bei der Aufbereitung von Medizinprodukten More |
