Alfresa
의료 서비스 제공자를 위한 제약 및 의료 제품
Alfresa는 처방약, 의료 제품 및 진단 용품을 유통합니다. 해당 네트워크는 일본 전역의 약국 및 의료 시설에 서비스를 제공합니다.
- Type
- Distributor
- Location
- Tokyo, Japan
- Website
- alfresa.com
- Categories
- 의약품 제조, 의료 및 건강 관리 용품
- Markets
- 일본
Verified facts
- sanctions-clear (green), checked 2026-08-04 OpenSanctions
- debarment-clear (green), checked 2026-08-04 OpenSanctions
- fda-registered (green), checked 2026-08-04 FDA
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- domain-registered (green), checked 2026-08-04 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
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)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)