ACDIMA International
Pan-Arabisch bedrijf voor farmaceutische en medische apparatuur, opgericht in 1976 door de Arabische Economische Eenheidsraad.
ACDIMA (Arabische onderneming voor geneesmiddelenindustrie en medische apparaten) werd op 6 maart 1976 opgericht bij resolutie van de Arabische Economische Eenheidsraad met een startkapitaal van 60 miljoen Koeweitse dinar. Het bedrijf brengt farmaceutische producten en die van haar dochterondernemingen op de markt in de Arabische wereld. De aangesloten bio-equivalentie CRO, ACDIMA Center, is gevestigd in Amman.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Amman, Jordan
- Founded
- 1976
- Website
- acdima.com
- Categories
- Medische en gezondheidszorgbenodigdheden
- Markets
- Verenigde Arabische Emiraten, Saoedi-Arabië, Egypte, Duitsland, Verenigd Koninkrijk
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)