LOTRIČ Meroslovje d.o.o.
Slovenian industrial manufacturer and exporter
LOTRIČ Meroslovje d.o.o. is listed by Sloexport in the automotive sector. Its directory profile describes operations including We have been calibrating, testing, verificating and certificating with a love for metrology for three decades. We develop state of the art, highly perfected, but easy to use metrology products and services. We transfer knowledge, represent top Slovene and foreign producers of measurement, pharmaceutical and laboratory.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Selca, Slovenia
- Website
- https://lotric.si
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies, Vehicle Parts & Accessories
- Markets
- Slovenia, Austria, Germany, Italy, Croatia
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
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- export-registered (green), checked 2026-08-09 EU EORI validation (European Commission)
- public-contract-awarded (green), effective since 2026-02-25 TED (Tenders Electronic Daily), EU public procurement award notices Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. Directive 2014/24/EU, Article 57 (exclusion grounds)
- registry-id-verified (green), checked 2026-08-16 Poslovni register Slovenije (AJPES)
- vat-valid (green), checked 2026-08-09 VIES
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)