Oura Health Oy
Финский производитель умных колец и устройств для здоровья.
Oura разрабатывает и производит Oura Ring , носимое устройство для сна, готовности, активности и здоровья. Основанная в Оулу в 2013 году, компания распространяет смарт-кольца среди потребителей, партнеров в сфере здравоохранения и корпоративных программ по всему миру.
- Type
- brand seeking distribution
- Location
- Oulu, Finland
- Founded
- 2013
- Website
- ouraring.com
- Categories
- Носимые устройства, Медицинские товары и расходники
- Markets
- Финляндия, Соединенные Штаты, Германия, Великобритания
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)