Stelion Specta
Stelion Specta

Register your company

For companies established in the EU or the EEA that place class I eyewear — spectacle frames, uncut finished lenses, ready-to-wear readers — on the EU market under Regulation (EU) 2017/745 (MDR).

Stelion Specta builds your technical file and your EUDAMED registration package from your own facts and your factory's documents, and explains each step before you approve it. Every sentence it writes carries its source.

Stelion Specta signs nothing, certifies nothing and declares nothing. The declaration of conformity is signed by a named person in your company; the obligations of the manufacturer remain yours.

As entered in the commercial register, including the legal form.
EU member states and EEA states. Stelion Specta does not yet serve companies established elsewhere.
First and last name of the person opening this account.
The confirmation link goes to this address; it becomes your sign-in name.
Your role under the MDR
This is your statement, not a determination. The first milestone checks it against your facts, with citations.

Importers (Article 2(33) MDR) and distributors (Article 2(34) MDR) cannot register yet; Stelion Specta serves manufacturers for now.

How Stelion Specta processes the data you enter here is described in the privacy notice. Customer data and model inference never leave the EU.

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