Genis hf.
ジーニスHF。は、輸出対応の B2B チャネル向けにキチンベースの原料を製造しています。
ジーニスHF。シグルフィヨルズルでキチンベースの原料、創傷ケア材料、海洋バイオテクノロジー製品を製造しています。 2005 年に設立された同社は、IS、NO、DK、米国および関連輸出市場の医療会社、サプリメント ブランド、成分販売業者、輸出パートナーに製品を供給しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Siglufjordur, Iceland
- Founded
- 2005
- Website
- genis.is
- Categories
- 医療およびヘルスケア用品, サプリメントとウェルネス
- Markets
- アイスランド, ノルウェー, デンマーク, アメリカ合衆国
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)