Medicop specialna oprema d.o.o.
Slovenian industrial manufacturer and exporter
Medicop specialna oprema d.o.o. is listed by Sloexport in the other manufacturing sector. Its directory profile describes operations including Company Medicop from Murska Sobota engaged in the production of medical equipment and outfitting of vehicles for special purposes. Years of experience and cooperation with users in the field of medical equipment in the field of medical gases in the hospitals and ambulances allow us to create professional people the bes.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Murska Sobota, Slovenia
- Website
- https://medicop.eu
- 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
- public-contract-awarded (green), checked 2026-08-03 TED, EU public procurement bulletin 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)
- lei-lapsed (amber), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
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