L I N E T spol. s r.o.
Товары медицинского назначения и здравоохранения, Чехия
Л И Н Е Т spol. с р.о. , компания, занимающаяся поставками медицинского оборудования и товаров для здоровья, базирующаяся в Сланах, Чехия. Внесен в государственный реестр предприятий.
- Type
- brand seeking distribution
- Location
- Slaný, Czechia
- Founded
- 1990
- Categories
- Медицинские товары и расходники
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 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)
- 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)