NeuroRehab Technologies OÜ
Page principale | Technologies de neuroréadaptation
Traitement efficace basé sur l'IA et la réalité virtuelle pour la douleur des membres fantômes, dont il a été prouvé qu'il réduit la douleur et rétablit la fonction.
- Type
- Manufacturer
- Location
- Kesklinna linnaosa, Estonia
- Founded
- 2024
- Website
- https://www.neurorehabtech.com
- Categories
- Fournitures médicales et de santé
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)