TECNOSERVICE EQUIPMENT S.R.L.
TECNOSERVICE EQUIPMENT S.R.L. - производитель из РО
TECNOSERVICE EQUIPMENT S.R.L. , производитель, расположенный по ул. Деж, номер. 40, код 012284, сектор 1, Бухарест, Румыния, Страда Деж 40, 012284 Бухарест, Румыния.
- Type
- brand seeking distribution
- Location
- Bucharest, Romania
- Website
- http://www.tecnos.ro/
- Categories
- Медицинские товары и расходники, Промышленные станки и машины
- Markets
- Румыния
Verified facts
- named-by-manufacturer (green), checked 2026-09-04 EVT - Eye Vision Technology GmbH distributor list
- public-contract-awarded (green), checked 2026-06-05 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)
- registry-activity (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- lei-lapsed (amber), checked 2026-08-30 GLEIF global LEI register (golden copy)
- registered-address (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- registry-active-global (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- registry-id-verified (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- leadership-on-record (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- registered-since (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
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)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission
- No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment