NeuroRehab Technologies OÜ
Trang chính | Công nghệ phục hồi thần kinh
Phương pháp điều trị hiệu quả dựa trên AI và VR đối với chứng đau chi ảo, đã được chứng minh là giúp giảm đau và phục hồi chức năng.
- Type
- Manufacturer
- Location
- Kesklinna linnaosa, Estonia
- Founded
- 2024
- Website
- https://www.neurorehabtech.com
- Categories
- Vật tư y tế và chăm sóc sức khỏe
Listed in a source registry
Verified facts
- domain-registered (green), checked 2026-07-27 Domain registry record
- registry-id-verified (green), checked 2026-07-27 e-Business Register (e-Ariregister), Centre of Registers and Information Systems (RIK)
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 2024-11-06 e-Äriregister (RIK)
- directors-on-file (green), checked 2026-08-24 e-Äriregister (RIK)
- leadership-on-record (green), checked 2024-11-06 e-Äriregister (RIK)
- ownership-on-record (green), checked 2026-08-24 e-Äriregister (RIK)
- annual-accounts-filed (green), checked 2026-08-07 e-Äriregister (majandusaasta aruanded)
- registered-manufacturer (green), checked 2026-08-06 e-Äriregister (teatatud tegevusalad)
- sanctions-clear (green), checked 2026-07-27 OpenSanctions
- registry-active-global (green), checked 2026-07-27 e-Äriregister
- debarment-clear (green), checked 2026-07-27 OpenSanctions
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)