ECHO razvojno tehnološki inženiring, d.o.o.
Fabricante e exportador industrial esloveno
ECHO razvojno tehnološki inženiring, d.o.o. é listada pela Sloexport no setor elétrico e eletrônico. Seu perfil de diretório descreve operações, incluindo a empresa ECHO Instruments, Ltd, uma empresa de tecnologia que desenvolve e fabrica sistemas de medição nas áreas de ecologia, medicina, farmácia e biotecnologia.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Slovenske Konjice, Slovenia
- Website
- https://echo.si
- Categories
- Fabricação farmacêutica, Suprimentos médicos e de saúde, Equipamentos elétricos e de energia
- Markets
- Eslovênia, Áustria, Alemanha, Itália, Croácia
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)