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
- 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
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
- vat-valid (green), checked 2026-08-09 VIES
- export-registered (green), checked 2026-08-09 EU EORI validation (European Commission)
- public-contract-awarded (green), checked 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)
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)
- 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)
- Vehicle parts affecting safety sold in Europe generally require UNECE type approval (E-mark). UNECE