ECHO razvojno tehnološki inženiring, d.o.o.
슬로베니아 산업 제조업체 및 수출업체
ECHO razvojno tehnološki inženiring, d.o.o. Sloexport는 전기 및 전자 부문에 상장되어 있습니다. 디렉토리 프로필에는 생태학, 의학, 약학, 생명공학 분야의 측정 시스템을 개발 및 제조하는 기술 회사인 ECHO Instruments company를 포함한 운영이 설명되어 있습니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Slovenske Konjice, Slovenia
- Website
- https://echo.si
- Categories
- 의약품 제조, 의료 및 건강 관리 용품, 전기 및 전력 장비
- Markets
- 슬로베니아, 오스트리아, 독일, 이탈리아, 크로아티아
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)