TECNOSERVICE EQUIPMENT S.R.L.
TECNOSERVICE EQUIPMENT S.R.L. - fabricant basé en RO
TECNOSERVICE EQUIPMENT S.R.L. est un fabricant situé à Str. Dej, nr. 40, cod 012284, Secteur 1, Bucuresti, Roumanie, Strada Dej 40, 012284 București, Roumanie.
- Type
- brand seeking distribution
- Location
- Bucharest, Romania
- Website
- http://www.tecnos.ro/
- Categories
- Fournitures médicales et de santé, Machines industrielles
- Markets
- Roumanie
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 Ici l'attribution porte aussi un contrôle fait par d'autres: dans l'UE et l'EEE, l'acheteur public doit exclure les candidats condamnés pour fraude, corruption ou blanchiment, ainsi que ceux dont une décision définitive a établi des dettes fiscales ou sociales. 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