AS Ldiamon
Tıbbi ve Sağlık Malzemeleri, Estonya
AS Ldiamon, Estonya merkezli bir tıbbi ve sağlık malzemeleri şirketidir. Kamu ticaret sicilinde listelenmiştir.
- Type
- Manufacturer
- Location
- Estonia
- Founded
- 2005
- Website
- https://www.ldiamon.eu
- Categories
- Tıbbi ve Sağlık Malzemeleri
Listed in a source registry
Verified facts
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 2005-07-11 e-Äriregister (RIK)
- directors-on-file (green), checked 2026-08-24 e-Äriregister (RIK)
- leadership-on-record (green), checked 2007-10-11 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 2026-07-09 e-Äriregister
- 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)