OÜ EQUA
Производство EQUA разделено на три направления: медицинская продукция, физиотерапевтическое оборудование и ветеринарная продукция. Медицина, физиотерапия и
Производство EQUA разделено на три направления: медицинская продукция, физиотерапевтическое оборудование и ветеринарная продукция. Медицина, физиотерапия и ветеринария
- Type
- Manufacturer
- Location
- Tartu linn, Estonia
- Founded
- 1997
- Website
- https://equa.ee
- Categories
- Медицинские товары и расходники
Listed in a source registry
Verified facts
- annual-accounts-filed (green), checked 2026-08-07 e-Äriregister (majandusaasta aruanded)
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 1997-09-01 e-Äriregister (RIK)
- directors-on-file (green), checked 2026-08-24 e-Äriregister (RIK)
- leadership-on-record (green), checked 1997-09-01 e-Äriregister (RIK)
- ownership-on-record (green), checked 2026-08-24 e-Äriregister (RIK)
- public-contract-awarded (green), checked 2025-07-16 TED (Tenders Electronic Daily), EU public procurement award notices Здесь награда несёт ещё и чужую проверку: в ЕС и ЕЭЗ заказчик обязан отстранить участника, осуждённого за мошенничество, коррупцию или отмывание, и того, за кем окончательным решением признаны долги по налогам или социальным взносам. Directive 2014/24/EU, Article 57 (exclusion grounds)
- registered-manufacturer (green), checked 2026-08-06 e-Äriregister (teatatud tegevusalad)
- sanctions-clear (green), checked 2026-07-27 OpenSanctions
- debarment-clear (green), checked 2026-07-27 OpenSanctions
- registry-active-global (green), checked 2026-07-27 e-Äriregister
- 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)