27.05.2021
Regulation 2017/745 – it has become a fact
The medical devices market had to wait a long time for regulatory changes Nearly 30 years after the entry into force of...
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28.10.2021
Ladies and Gentlemen,
We are proud to announce that today, after more than a year of assessment carried out jointly by the Ministry of Health and the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, we have received authorization in the scope of Directive 98/79/EC of the European Parliament and of th Council of October 27, 1998 on medical devices used for in vitro diagnostics. Within the next 2 months, we will be added to the NANDO database and thus we will become a notified body.
The decision and the scope of our authorization are available at this link – document
NewsDirector of the Sales and Marketing Department
CeCert Sp z o. o.