Bittium Corporation
Finse fabrikant van beveiligde apparaten, biosignalen en draagbare technologie.
Bittium ontwikkelt veilige communicatieapparatuur, biosignaalmeetsystemen, ECG-producten en verbonden medische technologie. Met wortels in de Finse elektronica sinds 1985, levert het bedrijf internationaal aan klanten in de gezondheidszorg, defensie en industrie.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Oulu, Finland
- Founded
- 1985
- Website
- bittium.com
- Categories
- Wearables en persoonlijke apparaten, Medische en gezondheidszorgbenodigdheden, Consumentenelektronica
- Markets
- Finland, Duitsland, Verenigde Staten, Verenigd Koninkrijk
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- registry-activity (green), checked 2026-09-18 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- registry-id-verified (green), checked 2026-09-18 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- tax-filing-active (green), checked 2026-09-18 Finnish Tax Administration, public corporate tax data 2024 (Verohallinto)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registered-address (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registry-active-global (green), checked 2026-07-09 Finnish Patent and Registration Office (PRH)
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)