DIN EN ISO 10993-5 [CURRENT] referenced in following documents:
| Document number | Edition | Title |
|---|---|---|
| DIN SPEC 13257 | 2019-09 | Single-use foot bandage in medical foot treatment - Requirements and test methods More |
| DIN SPEC 13259 | 2020-09 | Reusable venous tourniquets for hygienic blood sampling - Requirements More |
| DIN 13097-4 | 2019-06 | Hypodermic needles - Part 4: Point geometry, requirements and testing More |
| VDI 2017 | 2019-07 | Medical Grade Plastics (MGP) More |
| VDI 2083 Blatt 21 | 2019-10 | Cleanroom technology - Cleanliness of medical devices in the manufacturing process More |
| VDI 5701 | 2018-05 | Biomaterials in medicine - Classification, requirements, and applications More |
| VDI 5710 Blatt 1 | 2019-07 | Licensing and implementing of new nanotechnologies in the area of medical technology - Fundamentals More |
| DIN EN ISO 10993-1 | 2021-05 | Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10); German version EN ISO 10993-1:2020 More |
| DIN EN ISO 10993-4 | 2017-12 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017); German version EN ISO 10993-4:2017 More |
| DIN EN ISO 11135 | 2020-04 | Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018); German version EN ISO 11135:2014 + A1:2019 More |
