Dokumendiregister | Terviseamet |
Viit | 11.1-12/24/144-2 |
Registreeritud | 05.01.2024 |
Sünkroonitud | 27.03.2024 |
Liik | Väljaminev dokument |
Funktsioon | 11.1 Turustamise järgne järelevalve (post-marketing surveillance) |
Sari | 11.1-12 Turujärelevalvega seotud muu kirjavahetus („tahetakse infot“) - Nõustamine |
Toimik | 11.1-12/2023 |
Juurdepääsupiirang | Avalik |
Juurdepääsupiirang | |
Adressaat | 1M4 UG (haftungsbeschränkt) |
Saabumis/saatmisviis | 1M4 UG (haftungsbeschränkt) |
Vastutaja | Karl Kalev Türk (TA, Peadirektori asetäitja (1) vastutusvaldkond, Meditsiiniseadmete osakond) |
Originaal | Ava uues aknas |
From: "Meditsiiniseadmed (Medical Devices)" <[email protected]>
Sent: Mon, 18 Dec 2023 08:13:18 +0000
To: 1M4 UG - QM <[email protected]>
Subject: Vs: New request for e-consulting
Dear Sabina,
Thank you for your inquiry.
Here are the answers to your questions:
If the plan is to place devices on the EU market under your new Estonian company name, you will need to establish an Estonian company, as Kristi has previously guided you. There are no country-specific rules or requirements for appointing a PRRC. General PRRC principles apply as seen in the MDCG 2019-7.
Please see the aforementioned MDCG guidance – these principles apply.
Until EUDAMED is not fully functional, the placing on the market for class I devices goes through the national Medical Devices and Appliances Database, as stated in the Medical Device Act § 412:
Implementation of obligations and requirements related with European database on medical devices
Until the implementation date of the obligations set out in points d and e of subsection 3 of Article 122 of Regulation (EU) 2017/745 and in points a and f of subsection 3 of Article 113 of Regulation (EU) 2017/746 of the European Parliament and of the Council related with the European database on medical devices, the exchange of information with the Health Board and the transmission of data to the Health Board takes place according to the wording of the Medical Devices Act in force prior to entry into force of this wording.
The previous wording of the act can be found here, and the relevant paragraph is § 26 (1):
Any person who places a class I medical device, custom-made medical device, system of medical devices, procedure pack or in vitro diagnostic medical device on the market in Estonia, shall notify, at least ten days before the medical device is placed on the market, the Health Board of the intention to place the medical device on the market and of any significant alterations of the medical device.
English is accepted as the language for technical documentation.
Please do not hesitate to contact me for further information or any questions.
Best regards,
Karl Kalev Türk
Chief Specialist
Department of Medical Devices
Phone +372 5648 5663
[email protected] | [email protected]
Republic of Estonia Terviseamet | Health Board +372 794 3500 [email protected] 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: 1M4 UG - QM <[email protected]>
Saatmisaeg: laupäev, 16. detsember 2023 12:53
Adressaat: Karl Kalev Türk <[email protected]>
Teema: Fwd: New request for e-consulting
Tähelepanu! Tegemist on väljastpoolt asutust saabunud kirjaga. Tundmatu saatja korral palume linke ja faile mitte avada. |
Hello Karl!
I got your contact details from Kirsti (see below).
We - 1M4 UG - are a small company and sell/produce some medical and non-medical products. These are produced mostly in China and Pakistan, but we are the manufacturer of the medical devices. They are class I, so no notified body is needed.
We think about moving the company to Estonia. Could you please give me some advice like:
Where do we have the company as manufacturer, including PRRC?
Do you need a certificate / proof of training for PRRC?
Where do we have to register the medical devices? Eudamed is still not fully working.
In which language do you need the technical documentation? Is English ok or do you need it in Estonian?
Any advice you can give me according to MDR and this topic would be helpful for our decision.
Thank you very much!
Best regards
Sabina
1M4 UG (haftungsbeschränkt)
Strandweg 16
17213 Untergöhren - Deutschland
[email protected] - www.1m4.de
Steuer-Nr..: 075/108/94923
USt-IdNr.: DE323762513
Handelsregister HRB 20890
Amtsgericht Neubrandenburg
Sitz der Gesellschaft: Untergöhren
Geschäftsführer: Roland Ortloff
------- Weitergeleitete Nachricht ------
Von: Kirsti Priivits <[email protected]>
Datum: Fr. 24. Nov. 2023 um 13:11
Betreff: New request for e-consulting
An: 1M4 UG - QM <[email protected]>
Hallo Sabina,
Danke für Deine E-Mail und ich habe gleich verstanden, dass ein Termin noch in dieser Woche zu finden, schwierig sein wird.
Ich bin nächster Woche unterwegs - erst in Österreich und dann in Finland. Ich schlage vor, dass wir unser Intro in Dezember machen.
Doch kann ich gerne gleich einige Informationen teilen (auf Englisch, ich hoffe, dass es auch so passt):
First I am covering the topic of steps to take for establishing a company:
Holders of an Estonian ID card or e-Residency card and a growing number of EU member states’ ID cards can establish a Private Limited Company fully online. If an ID or e-Residency card is not available, a visit to a notary in Estonia is needed to verify the foundation documents.
Establishing a private limited company – as easy as ABC:
Though the process is fairly simple, specialized service providers (private companies) can help you through the steps. If using e-Residency, read suggestions how to choose a service provider and what services they can help you with.
I contacted Terviseamet (Estonian Health Board) and recieved advice to forward You directy to them. Please contact Karl Kalev Türk [email protected] to arrage a meeting.
Some information in english can be found here: Contacts: Medical Devices | Government installation profile (terviseamet.ee). There is a Medical Device Act in English available.
If You have any other questions, please let me know and let’s arrange intro in December.
Best regards,
Kirsti Priivits
Deputy Head of Global Business Development
Invest Estonia
Enterprise Estonia
+372 501 2063
Sepise 7, 11415 Tallinn
Building a successful Estonia!
Facebook: EAS – Enterprise Estonia
LinkedIn: EAS – Enterprise Estonia
From: 1M4 UG - QM <[email protected]>
Sent: Tuesday, November 21, 2023 5:25 PM
To: Kirsti Priivits <[email protected]>
Subject: Re: New request for e-consulting
Hallo Kirsti,
Danke für deine schnelle Rückmeldung. Morgen und übermorgen passt es bei mir leider nicht.
Aber ich melde mich, sobald ich etwas Puffer habe!
Gibt es denn allgemeine Infos, die ich vorab erhalten kann?
Vielen Dank!
Herzliche Grüße
Sabina
1M4 UG (haftungsbeschränkt)
Strandweg 16
17213 Untergöhren - Deutschland
[email protected] - www.1m4.de
Steuer-Nr..: 075/108/94923
USt-IdNr.: DE323762513
Handelsregister HRB 20890
Amtsgericht Neubrandenburg
Sitz der Gesellschaft: Untergöhren
Geschäftsführer: Roland Ortloff
Am Di., 21. Nov. 2023 um 15:52 Uhr schrieb Kirsti Priivits <[email protected]>:
Hallo Sabina,
Danke für deine E-Mail und Interesse in Estland dein Unternehmen zu gründen.
Ich bin Kirsti Priivits, verantwortlich für DACH Region in unserem Team.
Ich würde gerne eine Intro machen, uns vorstellen und von Dein Unternehmen und von Deine Pläne hören.
Wie würde Dir morgen, am Mittwoch um 13.00 EET oder am Donnerstag um 10.00 EET passen?
Freundliche Grüsse,
Kirsti Priivits
Deputy Head of Global Business Development
Invest Estonia
Enterprise Estonia
+372 501 2063
Sepise 7, 11415 Tallinn
Building a successful Estonia!
Facebook: EAS – Enterprise Estonia
LinkedIn: EAS – Enterprise Estonia
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Nimi | K.p. | Δ | Viit | Tüüp | Org | Osapooled |
---|---|---|---|---|---|---|
Vastuskiri | 07.02.2024 | 49 | 11.1-12/24/144-9 | Sissetulev dokument | ta | 1M4 UG (haftungsbeschränkt) |
Vastuskiri | 06.02.2024 | 50 | 11.1-12/24/144-8 | Väljaminev dokument | ta | 1M4 UG (haftungsbeschränkt |
Vastuskiri | 06.02.2024 | 50 | 11.1-12/24/144-7 | Sissetulev dokument | ta | 1M4 UG (haftungsbeschränkt |
Vastuskiri | 10.01.2024 | 77 | 11.1-12/24/144-6 | Väljaminev dokument | ta | 1M4 UG (haftungsbeschränkt) |
Kiri | 10.01.2024 | 77 | 11.1-12/24/144-5 | Sissetulev dokument | ta | 1M4 UG (haftungsbeschränkt) |
Kiri | 05.01.2024 | 82 | 11.1-12/24/144-3 | Sissetulev dokument | ta | 1M4 UG (haftungsbeschränkt) |
Kiri | 05.01.2024 | 82 | 11.1-12/24/144-4 | Väljaminev dokument | ta | 1M4 UG (haftungsbeschränkt) |
Kiri | 05.01.2024 | 82 | 11.1-12/24/144-1 | Sissetulev dokument | ta | 1M4 UG (haftungsbeschränkt) |