Kiri

To whom it may concern,

I am writing to clarify if the IFU (patient leaflets), packagings and labels of medical devices are to be applied the same terms and requirements as in Latvia, namely, they are subject to the Regulations 2017/745,  2017/746? Or are there any additional requirements from Estonian national authority.

 We have an array of medical devices that we would like to distribute also in Estonia.

Thank you very much in advance for your answer,

Respectfully,