L I N E T spol. s r.o.
Fournitures médicales et de santé, Tchéquie
L I N E T spol. s.r.o. est une entreprise de fournitures médicales et de soins de santé basée à Slaný, en Tchéquie. Inscrite au registre public des entreprises.
- Type
- brand seeking distribution
- Location
- Slaný, Czechia
- Founded
- 1990
- Categories
- Fournitures médicales et de santé
Listed in a source registry
Verified facts
- export-registered (green), checked 2026-08-12 EU EORI validation (European Commission)
- public-contract-awarded (green), checked 2026-08-17 TED, EU public procurement bulletin 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)
- workforce-on-record (green), checked 2026-08-16 ARES, registr ekonomických subjektů (Česká republika)
- ownership-on-record (green), checked 2026-08-13 GLEIF global LEI index
- vat-valid (green), checked 2026-08-08 VIES (European Commission)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- registry-active-global (green), checked 2026-08-24 ARES (Czech business register)
- registered-since (green), checked 1990-09-03 ARES (Czech business register)
- directors-on-file (green), checked 2026-08-24 ARES (Czech business register)
- leadership-on-record (green), checked 2016-11-10 ARES (Czech business register)
- registry-activity (green), checked 1990-09-03 ARES (Czech business register)
- registry-id-verified (green), checked 2026-07-04 ARES (Ministry of Finance) + Verejny rejstrik a Sbirka listin (Ministry of Justice)
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)