L-TEK elektronika d.o.o.
Sloven endüstriyel üretici ve ihracatçı
L-TEK elektronika d.o.o. Elektrik ve elektronik sektöründe Sloexport tarafından listelenmektedir. Dizin profili, L-Tek d.o.o. dahil olmak üzere işlemleri açıklar. geniş bir endüstri yelpazesi için elektronik çözümlerin araştırma ve geliştirmesine, prototiplenmesine ve üretimine odaklanmış, kapsamlı EMS çözümlerinin tanınmış bir sağlayıcısıdır. Hizmetleri ağırlıklı olarak ölçüm teknolojisi, tıbbi cihazlar, endüstriyel sensörler ve E-mobilite alanlarında mevcuttur. Oldu.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Šentjernej, Slovenia
- Website
- https://l-tek.com
- Categories
- İlaç Üretimi, Tıbbi ve Sağlık Malzemeleri, Elektrik ve Güç Ekipmanları
- Markets
- Slovenya, Avusturya, Almanya, İtalya, Hırvatistan
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)