L-TEK elektronika d.o.o.
Словенский промышленный производитель и экспортер
Л-ТЕК электроника о.о.о. котируется Sloexport в секторе электротехники и электроники. Его профиль каталога описывает операции, включая L-Tek d.o.o. , известный поставщик комплексных решений EMS, специализирующийся на исследованиях и разработках, прототипировании и производстве электронных решений для широкого спектра отраслей. Ее услуги в основном представлены в области измерительных технологий, медицинского оборудования, промышленных датчиков и электронной мобильности. Это было.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Šentjernej, Slovenia
- Website
- https://l-tek.com
- Categories
- Фармацевтическое производство, Медицинские товары и расходники, Электротехника и силовое оборудование
- Markets
- Словения, Австрия, Германия, Италия, Хорватия
Listed in a source registry
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
- domain-registered (green), checked 2026-08-09 Domain registry record
- export-registered (green), checked 2026-08-09 EU EORI validation (European Commission)
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- vat-valid (green), checked 2026-08-09 VIES
- registry-activity (green), checked 2026-08-16 Seznam davčnih zavezancev (FURS, Finančna uprava RS)
- registry-id-verified (green), checked 2026-08-16 Poslovni register Slovenije (AJPES)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
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)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)