ECHO razvojno tehnološki inženiring, d.o.o.
Słoweński producent i eksporter przemysłowy
ECHO razvojno tehnološki inženiring, d.o.o. jest notowana na giełdzie Sloexport w branży elektrycznej i elektronicznej. Jej profil katalogowy opisuje działalność m.in. firmy ECHO Instruments, Ltd. jest firmą technologiczną opracowującą i produkującą systemy pomiarowe w dziedzinach ekologii, medycyny, farmacji i biotechnologii.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Slovenske Konjice, Slovenia
- Website
- https://echo.si
- Categories
- Produkcja farmaceutyczna, Artykuły medyczne i związane z opieką zdrowotną, Sprzęt elektryczny i zasilający
- Markets
- Słowenia, Austria, Niemcy, Włochy, Chorwacja
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)