Oura Health Oy
Fabricant finlandais de bagues intelligentes et de vêtements de santé.
Oura conçoit et fabrique l'Oura Ring, un appareil portable pour le sommeil, la préparation, l'activité et les informations sur la santé. Fondée à Oulu en 2013, la société distribue des bagues intelligentes aux consommateurs, aux partenaires de bien-être et aux programmes d'entreprise du monde entier.
- Type
- brand seeking distribution
- Location
- Oulu, Finland
- Founded
- 2013
- Website
- ouraring.com
- Categories
- Objets connectés et portables, Fournitures médicales et de santé
- Markets
- Finlande, États-Unis, Allemagne, Royaume-Uni
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- vat-valid (green), checked 2026-07-09 VIES
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-active-global (green), checked 2026-07-09 Finnish Patent and Registration Office (PRH)
- places-goods-on-market (green), checked 2026-08-30 Registre national des producteurs (ADEME/SYDEREP), France
- registered-address (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- tax-filing-active (green), checked 2026-08-14 Finnish Tax Administration, public corporate tax data 2024 (Verohallinto)
- registry-id-verified (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registry-activity (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
Claimed certifications
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)