UŽDAROJI AKCINĖ BENDROVĖ "INTERSURGICAL"
Forniture mediche e sanitarie, Lituania
La SOCIETÀ A RESPONSABILITÀ LIMITATA "INTERSURGICAL" è una società di forniture mediche e sanitarie con sede a Švenčionių, Lituania. Iscritta in un registro pubblico delle imprese.
- Type
- brand seeking distribution
- Location
- Švenčionių, Lithuania
- Categories
- Forniture medicali e sanitarie
Listed in a source registry
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 Qui l'aggiudicazione porta con sé anche un controllo altrui: nell'UE e nello SEE la stazione appaltante deve escludere gli operatori condannati per frode, corruzione o riciclaggio e quelli con debiti fiscali o contributivi accertati con decisione definitiva. 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)