TECNOSERVICE EQUIPMENT S.R.L.
テクノサービス・エキップメント S.R.L. - ROに拠点を置くメーカー
テクノサービス・エキップメント S.R.L.はStrにあるメーカーです。デジ、nr. 40、cod 012284、セクター 1、ブカレスト、ルーマニア、Strada Dej 40、012284 ブカレスト、ルーマニア。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Bucharest, Romania
- Website
- http://www.tecnos.ro/
- Categories
- 医療およびヘルスケア用品, 産業機械
- Markets
- ルーマニア
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- public-contract-awarded (green), effective since 2026-06-05 TED (Tenders Electronic Daily), EU public procurement award notices ここでの落札は、他者による審査も伴います。EUおよびEEAでは、公共調達者は詐欺、汚職、資金洗浄で有罪となった入札者、および確定した決定で税や社会保険料の未納が認定された入札者を排除しなければなりません。 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)
- named-by-manufacturer (green), effective since 2026-06-28 EVT - Eye Vision Technology GmbH distributor list
- registered-address (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)
- registry-active-global (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- lei-lapsed (amber), checked 2026-09-07 GLEIF global LEI register (golden copy)
- 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