EMF - FURLAN & CO d.o.o., Ljubljana
منتج ومصدر صناعي سلوفيني
EMF - FURLAN & CO d.o.o., Ljubljana مدرجة في قائمة Sloexport في قطاع الكهرباء والإلكترونيات. يصف ملف تعريف الدليل الخاص به العمليات بما في ذلك إنتاج الأجهزة الطبية وتمثيلها وبيعها وصيانتها.
- Type
- Manufacturer
- Location
- Ljubljana, Slovenia
- Website
- https://emf-furlan.si
- Categories
- تصنيع الأدوية, اللوازم الطبية والرعاية الصحية, المعدات الكهربائية والطاقة
- Markets
- سلوفينيا, النمسا, ألمانيا, إيطاليا, كرواتيا
Listed in a source registry
Verified facts
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- domain-registered (green), checked 2026-08-08 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- lei-active (green), checked 2026-08-08 GLEIF
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)