EMF - FURLAN & CO d.o.o., Ljubljana

Does it exist and operate now?

• Contact matches countryThe phone code on their own site matches the country on file.Phone country code on their own site
• Registered company type: Limited liability companyThe legal form recognised in its own country.

Is it really a manufacturer?

• Registered in the state craft registerShows it makes goods itself; resellers are not admitted to this register.Sloexport Slovenian exporter directory

Is it safe to deal with?

• Not on sanctions listsShows no trading ban. Says nothing about reputation.Aug 2026OpenSanctions
• Not banned from public contractsShows it has not been barred from public contracts for misconduct.Aug 2026OpenSanctions

Do independent sources agree?

Is it reachable and responsive?

• Business email on the company's own domainSuggests an established business rather than a free mailbox.Aug 2026Mail server of the company domain

About

In the company's own words. We have not verified these claims.

EMF - FURLAN & CO d.o.o., Ljubljana is listed by Sloexport in the electrical and electronics sector. Its directory profile describes operations including Production, representation, sale and maintenance of medical devices.

Categories

Pharmaceutical ManufacturingMedical & Healthcare SuppliesElectrical & Power Equipment

Primary markets

🇸🇮 Slovenia 🇦🇹 Austria 🇩🇪 Germany 🇮🇹 Italy 🇭🇷 Croatia

Explore

Distributors in SloveniaPharmaceutical Manufacturing in SloveniaMedical & Healthcare Supplies in SloveniaElectrical & Power Equipment in Slovenia

Rules that apply to these goods

Regulations that commonly apply to shipments in this sector. Not legal advice: verify against the linked official source.

• 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)