HORIBA
분석 기기, 측정 시스템 및 진단 장치.
HORIBA는 교토 사업장에서 분석 장비, 측정 시스템 및 진단 장치를 제조합니다. 이 회사는 나열된 주요 시장 전반에 걸쳐 국내 구매자, OEM 고객, 소매업체 또는 수출 채널에 서비스를 제공합니다.
- Type
- Manufacturer
- Location
- Kyoto, Japan
- Founded
- 1945
- Website
- horiba.com
- Categories
- 산업기계, 의료 및 건강 관리 용품
- Markets
- 일본, 미국, 독일, 중국
Verified facts
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- fda-contract-manufacturer (green), checked 2026-08-08 FDA
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- fda-registered (green), checked 2026-08-08 FDA
- domain-registered (green), checked 2026-08-08 Domain registry record
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
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)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission