Genis hf.
제니스HF. 수출용 B2B 채널을 위한 키틴 기반 성분을 제조합니다.
제니스HF. Siglufjordur에서 키틴 기반 성분, 상처 치료 재료 및 해양 생명 공학 제품을 제조합니다. 2005년에 설립된 이 회사는 IS, NO, DK, 미국 및 관련 수출 시장 전반에 걸쳐 의료 회사, 보충제 브랜드, 성분 유통업체 및 수출 파트너에게 제품을 공급합니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Siglufjordur, Iceland
- Founded
- 2005
- Website
- genis.is
- Categories
- 의료 및 건강 관리 용품, 보충제 및 웰니스
- Markets
- 아이슬란드, 노르웨이, 덴마크, 미국
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 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
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)