UŽDAROJI AKCINĖ BENDROVĖ "INTERSURGICAL"

Listed in a source registry

Lithuania Sodra employer register (atvira.sodra.lt)

Verified facts

• registry-id-verified (green), checked 2026-09-02 Juridinių asmenų registras (Registrų centras)
• registered-since (green), checked 1994-09-13 Juridinių asmenų registras (Registrų centras)
• registry-active-global (green), checked 2026-09-02 Juridinių asmenų registras (Registrų centras)
• supervised-operator (green), checked 2026-08-16 Licencijų informacinė sistema, LIS (Registrų centras, Lietuvos atvirų duomenų portalas)
• aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
• registered-address (green), checked 2026-09-02 Juridinių asmenų registras (Registrų centras)
• public-contract-awarded (green), checked 2026-08-06 TED (Tenders Electronic Daily), EU public procurement award notices Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. Directive 2014/24/EU, Article 57 (exclusion grounds)
• lei-lapsed (amber), checked 2026-08-30 GLEIF global LEI register (golden copy)
• workforce-on-record (green), checked 2026-08-16 Valstybinio socialinio draudimo fondo valdyba (Sodra), atviri įmonių duomenys

Claimed certifications

• AEO, Authorised Economic Operator EU AEO database

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)

Check independently

• Sanctions and watchlists (OpenSanctions)