ACDIMA International
1976년 아랍경제통일협의회(Arab Economic Unity Council)에 의해 설립된 범아랍 제약 및 의료 기기 회사입니다.
ACDIMA(아랍 의약품 산업 및 의료 기기 회사)는 1976년 3월 6일 초기 자본금 6천만 쿠웨이트 디나르로 아랍경제통합위원회의 결의에 따라 설립되었습니다. 이 회사는 아랍 세계에서 의약품과 그 자회사의 제품을 판매합니다. 계열 생물학적 동등성 CRO인 ACDIMA 센터가 암만에 위치하고 있습니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Amman, Jordan
- Founded
- 1976
- Website
- acdima.com
- Categories
- 의료 및 건강 관리 용품
- Markets
- 아랍에미리트, 사우디아라비아, 이집트, 독일, 영국
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 2026-08-03 Mail server of the company domain
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-03 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-03 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- domain-registered (green), checked 2026-08-03 Domain registry record
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)