Dokumendiregister | Terviseamet |
Viit | 11.1-2/24/6100-2 |
Registreeritud | 06.06.2024 |
Sünkroonitud | 07.06.2024 |
Liik | Väljaminev dokument |
Funktsioon | 11.1 Turustamise järgne järelevalve (post-marketing surveillance) |
Sari | 11.1-2 Kirjavahetus Eesti turule lastavatest/kasutusele võetavatest/levitatavatest seadmetest MSA kaudu teavitamiseks |
Toimik | 11.1-2/2023 |
Juurdepääsupiirang | Avalik |
Juurdepääsupiirang | |
Adressaat | Scanex Medical Systems |
Saabumis/saatmisviis | Scanex Medical Systems |
Vastutaja | Karl Kalev Türk (TA, Peadirektori asetäitja (1) vastutusvaldkond, Meditsiiniseadmete osakond) |
Originaal | Ava uues aknas |
From: "Meditsiiniseadmed (Medical Devices)" <[email protected]>
Sent: Thu, 23 Feb 2023 10:03:50 +0000
To: Tuija Naumanen <[email protected]>
Subject: Vs: Assistance needed
Dear Tuija,
Thank you for your letter.
The distribution notification requirement in Estonia is based on Estonian Medical Devices Act § 26 (4) (https://www.riigiteataja.ee/en/eli/ee/524012023001/consolide/current) which says:
Every undertaking who distributes on the market of Estonia a system or procedure pack of medical devices according to Article 22 of Regulation (EU) 2017/745 of the European Parliament and of the Council or a class IIa, IIb or III medical device classified according to Regulation (EU) 2017/745 of the European Parliament and of the Council or Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical or Council Directive 93/42/EEC concerning medical devices or class B, C or D in vitro diagnostic medical devices classified according to Annex VIII of Regulation (EU) 2017/746 of the European Parliament and of the Council, shall notify the Health Board thereof within 10 days after distribution of the relevant medical device for the first time.
The distribution notification can be done through Estonian Medical Device Database (EMDDB, https://msa.sm.ee/).
For actors outside of Estonia we can make an account manually, so it is possible to log into the database with username and password. For creating an account we need a contact person’s full name, e-mail and the position in the company. Therefore, does the account go to your name?
Documents with the notifications of medical devices are following: Declaration of conformity, EC certificate, instruction for use in English, instruction for use in Estonian and copy of the labelling or packaging.
Also, please use a short guide for using the Estonian Medical Device Database that can be found on database homepage under „Forms“.
NB! Please note that the access to the database is limited to users outside of Estonia.
In case of this, please contact with [email protected] with an request to access to the database and your IP address. They will white-list your IP and you should have an access to the database.
This is a temporary restriction for security reasons which hopefully will be removed in near future.
Please do not hesitate to contact me for further information or any questions.
Best regards,
Karl Kalev Türk
peaspetsialist
meditsiiniseadmete osakond
+372 5648 5663
Republic of Estonia
Health Board
+372 794 3500
www.terviseamet.ee
Paldiski mnt 81, 10614 Tallinn
Estonia
This e-mail is confidential and meant for use by the person named in the letterhead. Any use in any way or copying of it by a person not marked as the addressee thereof is prohibited. If you have got this e-mail by mistake, please notify of it the sender without delay and delete the received e-mail together with all its attachments.
Saatja: Tuija Naumanen <[email protected]>
Saatmisaeg: teisipäev, 21. veebruar 2023 11:45
Adressaat: Meditsiiniseadmed (Medical Devices) <[email protected]>
Teema: Assistance needed
Good morning from Finland!
I would like to register Fotona lasers in Your system. Can You please advise me how to do it.
Thank You in advance!
Tuija
__________________________________
Tuija Naumanen
+358 (0) 40 520 6962
[email protected]
Gunskogantie 108 | FI-21600 Parainen
__________________________________
This communication is intended for the person(s) named above only. It contains information that is confidential and legally privileged. If received in error, please delete this e-mail and notify the sender. Thank you for your cooperation.
Nimi | K.p. | Δ | Viit | Tüüp | Org | Osapooled |
---|---|---|---|---|---|---|
Vastuskiri | 06.06.2024 | 1 | 11.1-2/24/6100-4 🔒 | Väljaminev dokument | ta | Scanex Medical Systems |
Kiri | 06.06.2024 | 1 | 11.1-2/24/6100-1 | Sissetulev dokument | ta | Scanex Medical Systems |
Kiri | 06.06.2024 | 1 | 11.1-2/24/6100-3 🔒 | Sissetulev dokument | ta | Scanex Medical Systems |