ECHO razvojno tehnološki inženiring, d.o.o.
Sloven endüstriyel üretici ve ihracatçı
ECHO, teknik açıdan etkileyici, d.o.o. Elektrik ve elektronik sektöründe Sloexport tarafından listelenmektedir. Dizin profili, ekoloji, tıp, eczacılık ve biyoteknoloji alanlarında ölçüm sistemleri geliştiren ve üreten bir teknoloji şirketi olan ECHO Instruments Company Ltd dahil olmak üzere operasyonları açıklamaktadır.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Slovenske Konjice, Slovenia
- Website
- https://echo.si
- Categories
- İlaç Üretimi, Tıbbi ve Sağlık Malzemeleri, Elektrik ve Güç Ekipmanları
- Markets
- Slovenya, Avusturya, Almanya, İtalya, Hırvatistan
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 2026-08-08 Domain registry record
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- lei-active (green), checked 2026-08-08 GLEIF
Import rules for these goods
- 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)
- 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)