ACDIMA International
Perusahaan farmasi dan peralatan medis Pan-Arab didirikan tahun 1976 oleh Dewan Persatuan Ekonomi Arab.
ACDIMA (Perusahaan Arab untuk Industri Obat dan Peralatan Medis) didirikan pada tanggal 6 Maret 1976 berdasarkan resolusi Dewan Persatuan Ekonomi Arab dengan modal awal 60 juta Dinar Kuwait. Perusahaan ini memasarkan produk farmasi dan anak perusahaannya di dunia Arab. CRO bioekivalensi yang berafiliasi, ACDIMA Center, berbasis di 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
- Perlengkapan Medis & Kesehatan
- Markets
- Uni Emirat Arab, Arab Saudi, Mesir, Jerman, Inggris Raya
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)