![IvDO](https://cdn.slatesource.com/b/3/5/b356860d-991b-40a4-a5fe-c026bc09c53a.webp)

# IvDO

- [Made in Slatesource](https://slatesource.com/@steph/ivdo)
- By [Steph](https://slatesource.com/@steph)
- Created on Aug 13, 2026

## IvDO

SR 812.219 — Ordinance of 26 May 2022 on In Vitro Diagnostic Medical Devices (IvDO) of 4 May 2022.

[fedlex.data.admin.ch](https://fedlex.data.admin.ch/eli/cc/2022/291?utm_source=slatesource)

English is not an official language of the Swiss Confederation. This translation is provided for information purposes only and has no legal force. English consolidation of 1 July 2026, which is also the date of the current binding text.

[fedlex.data.admin.ch](https://fedlex.data.admin.ch/eli/cc/2022/291?utm_source=slatesource)

## Preamble

The Swiss Federal Council, based on the Therapeutic Products Act of 15 December 2000 (TPA), Article 21 number 2 of the Electricity Act of 24 June 1902, Article 5 of the Metrology Act of 17 June 2011, Article 4 paragraph 1 of the Federal Act of 12 June 2009 on Product Safety, Article 37 paragraph 1 of the Radiological Protection Act of 22 March 1991 andin implementation of the Federal Act of 6 October 1995 on Technical Barriers to Trade, ordains:

SR 812.21 SR 734.0 SR 941.20 SR 930.11 SR 814.50 SR 946.51

## Contents

1\. General provisions — 5 articles 2. Making available on the Market and Putting into Service — 11 articles 3. Conformity Assessment, Certificate and Declaration — 9 articles 4. Designated Bodies — 13 articles 5. Requirements for Economic Operators — 10 articles 6. Device Surveillance — 12 articles 7. Conduct in relation to Devices — 5 articles 8. Market Surveillance — 6 articles 9. Data Processing — 2 articles 10. Final Provisions — 18 articles

[Official text on Fedlex — consolidation of 1 July 2026](https://fedlex.data.admin.ch/filestore/fedlex.data.admin.ch/eli/cc/2022/291/20260701/en/html/fedlex-data-admin-ch-eli-cc-2022-291-20260701-en-html.html?utm_source=slatesource)