Arterium Corporation
CEE市場向けに6つの治療薬ラインを持つウクライナの製薬メーカー。
Arterium は、キエフの施設で心臓血管薬、抗炎症薬、鎮痛薬、呼吸器薬を製造しています。グループ DF の一部として 2007 年に設立された同社は、ウクライナと CIS 全域の薬局チェーン、病院販売代理店、ヘルスケア卸売業者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
- Kyiv, Ukraine
- Founded
- 2007
- Website
- arterium.ua
- Categories
- 医療およびヘルスケア用品
- Markets
- ウクライナ, モルドバ, ジョージア, トルコ
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
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- domain-registered (green), checked 2026-08-04 Domain registry record
- sanctions-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- 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)