We use cookies to make our website more user-friendly and to continually improve it. Please agree to the use of cookies in order to proceed with using our websites. More information can be found in our data protection information and our cookie guidelines.

- Required
- Functional
- Personalization
- Required
  These cookies are essential for the operation of the site and enable, for example, security-relevant functions. In addition, we can also use this type of cookie to determine whether you want to remain logged in to your profile in order to make our services available to you more quickly when you visit our website again.
- Functional
  In order to further improve our offer and our website, we collect anonymized data for statistics and analysis. With the help of these cookies we can, for example, determine the number of visitors and the effect of certain pages on our website and optimize our content.
- Personalization
  We use these cookies to make it easier for you to use the site. For example, based on a previous (e.g. product search), you can conveniently access it when you visit our website again.

Attention: Your browser doesn't support javascript or you have deactivated Javascript in your browser. Please enable Javascript in your browser in order to be able to use all functions of this website.

Hydrogen Technologies Standards form the basic framework for market ramp-up
More information
Climate change Standards and specifications support climate targets
More information
Smart Farming Standards and specifications are drivers for the digitalization of agriculture
More information

Publications of NA 027-07-12 AA

Sort by:


DIN EN ISO 10993-16	2018-02	Standards	Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017); German version EN ISO 10993-16:2017 More	Order from DIN Media
DIN EN ISO 10993-17	2024-02	Standards	Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023); German version EN ISO 10993-17:2023 More	Order from DIN Media
DIN EN ISO 10993-17/A1	2024-09	Draft standard	Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents - Amendment 1 (ISO 10993-17:2023/DAM 1:2024); German and English version EN ISO 10993-17:2023/prA1:2024 More	Order from DIN Media
DIN EN ISO 10993-18	2023-11	Standards	Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020 + Amd 1:2022); German version EN ISO 10993-18:2020 + A1:2023 More	Order from DIN Media
DIN EN ISO 10993-23	2021-10	Standards	Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021); German version EN ISO 10993-23:2021 More	Order from DIN Media
DIN EN ISO 10993-23/A1	2024-10	Draft standard	Biological evaluation of medical devices - Part 23: Tests for irritation - Amendment 1: Additional in vitro reconstructed human epidermis models (ISO 10993-23:2021/DAM 1:2024); German and English version EN ISO 10993-23:2021/prA1:2024 More	Order from DIN Media
ISO/TR 10993-22	2017-07	Technical rule	Biological evaluation of medical devices - Part 22: Guidance on nanomaterials More	Order from DIN Media
ISO/TR 10993-33	2015-03	Technical rule	Biological evaluation of medical devices - Part 33: Guidance on tests to evaluate genotoxicity - Supplement to ISO 10993-3 More	Order from DIN Media
ISO/TR 10993-55	2023-02	Technical rule	Biological evaluation of medical devices - Part 55: Interlaboratory study on cytotoxicity More	Order from DIN Media
ISO/TR 21582	2021-07	Technical rule	Pyrogenicity - Principles and methods for pyrogen testing of medical devices More	Order from DIN Media

3 / 6

TOP

Want to learn more?

Show

Preferred form of address

Male

Female

Neutral

First name*

Last name*

E-mail*

Phone no.

Subject

???din.label.contact.mailSubject???

Message*

Security code*

Here you can find our privacy policy

*Required field