Osaühing MEDIFUR
Sản phẩm sức khỏe. Sản xuất và kinh doanh bàn massage. Kinh nghiệm từ năm 2003
Sản phẩm sức khỏe. Sản xuất và kinh doanh bàn massage. Kinh nghiệm từ năm 2003
- Type
- Manufacturer
- Location
- Sõmeru küla, Estonia
- Founded
- 2003
- Website
- www.medifur.ee
- Categories
- Vật tư y tế và chăm sóc sức khỏe
Listed in a source registry
Verified facts
- lei-lapsed (amber), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 2003-12-17 e-Äriregister (RIK)
- directors-on-file (green), checked 2026-08-24 e-Äriregister (RIK)
- leadership-on-record (green), checked 2011-10-24 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)
- registry-active-global (green), checked 2026-07-27 e-Äriregister
- debarment-clear (green), checked 2026-07-27 OpenSanctions
- sanctions-clear (green), checked 2026-07-27 OpenSanctions
- registry-id-verified (green), checked 2026-07-27 e-Business Register (e-Ariregister), Centre of Registers and Information Systems (RIK)
- tax-filing-active (green), checked 2026-08-15 Estonian Tax and Customs Board, open data on taxes paid
- workforce-on-record (green), checked 2026-08-15 Estonian Tax and Customs Board, open data on taxes paid
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)