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
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ
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 यहाँ ठेका मिलना किसी और की जाँच भी साथ लाता है: यूरोपीय संघ और ईईए में सार्वजनिक क्रेता को धोखाधड़ी, भ्रष्टाचार या धनशोधन में दोषी बोलीदाताओं को, और अंतिम निर्णय से कर या सामाजिक अंशदान बकाया पाए गए बोलीदाताओं को बाहर करना अनिवार्य है। 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)