CHIRON Group SE
수직형 머시닝센터 및 적층가공 시스템 제조업체.
CHIRON은 의료, 자동차, 항공우주 산업의 정밀 금속 가공을 위한 고속 수직 머시닝 센터와 적층 제조 시스템을 제조합니다. 회사는 직접 판매 및 기술 제휴를 통해 전세계로 수출하고 있습니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Tuttlingen, Germany
- Website
- chiron-group.com
- Categories
- 의료 및 건강 관리 용품, 차량 부품 및 액세서리, 금속, 철강 및 광업
- Markets
- 독일, 미국, 중국, 폴란드
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 2026-08-02 Domain registry record
- web-presence-since (green), checked 2026-08-02 Internet Archive (Wayback)
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- vat-valid (green), checked 2026-08-18 VIES (European Commission)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Profiles
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management 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)
- EU imports of iron, steel and aluminium goods are in the CBAM carbon-border regime: from 1 Jan 2026 importers need CBAM authorisation and must buy certificates. European Commission (CBAM)