OÜ EQUA
EQUA toodang jaguneb kolme valdkonna vahel: meditsiini tooted, füsioteraapia vahendid ning veterinaaria tooted. Meditsiin, füsioteraapia ja
EQUA toodang jaguneb kolme valdkonna vahel: meditsiini tooted, füsioteraapia vahendid ning veterinaaria tooted. Meditsiin, füsioteraapia ja veterinaaria
- Type
- Manufacturer
- Location
- Tartu linn, Estonia
- Founded
- 1997
- Website
- https://equa.ee
- Categories
- 의료 및 건강 관리 용품
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 여기서 낙찰은 남이 한 심사까지 함께 뜻합니다. EU와 EEA에서는 공공 발주자가 사기, 부패, 자금세탁으로 유죄가 확정된 입찰자와 최종 결정으로 세금 또는 사회보험료 체납이 확인된 입찰자를 반드시 배제해야 합니다. 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)