Due to the number of questions coming from clients and potential clients, this is to inform that 3EC International a.s. has filed an Application for designation as notified body under the medical devices Regulation (MDR). Designation and notification process was initiated and you will be informed about the notification in the NANDO database.
3EC International a.s. filed an Application for designation as notified body under the Regulation (EU) 2017/745 on medical devices (MDR)
Archive
- OZNAM: Usmernenie k posudzovaniu zhody/ certifikácii výrobkov „Textilné ochranné rúška“ 16. 03. 2020
- What you need to know: MEDICAL DEVICES CHANGE OF LEGISLATION 03. 02. 2020
- MDR TRAINING COURSE - GET READY FOR MDR BY NB2265 30. 01. 2020
- On-site joint assessment conducted at 3EC International a.s. as per Regulation (EU) 2017/745 on medical devices (MDR) 14. 08. 2019
- 3EC International a.s. filed an Application for designation as notified body under the Regulation (EU) 2017/745 on medical devices (MDR) 05. 10. 2018
- NOVÁ NORMA ISO 45001:2018 03. 09. 2018
- Information to the clients regarding the BREXIT 31. 05. 2018
- Bonitný podnik 3EC International a.s. 06. 02. 2018
- 3EC International a.s. is accredited for EN ISO 13485: 2016 standard. 11. 12. 2017
- Going Concern 3EC International 19. 11. 2015
