Capital Diamond Star Group
قامت ميانمار بتنويع أعمالها في مجالات الأغذية والأدوية وتجارة التجزئة
تعد مجموعة Capital Diamond Star Group واحدة من التكتلات الأكثر احترامًا في ميانمار حيث يعمل بها أكثر من 9000 موظف في قطاعات تصنيع الأغذية وطحن الدقيق وتوزيع الرعاية الصحية وتجارة التجزئة والخدمات المالية وقطاعات السيارات.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Yangon, Myanmar
- Founded
- 1960
- Website
- cdsg.com.mm
- Categories
- الآلات الصناعية, المأكولات المتخصصة والذواقة, اللوازم الطبية والرعاية الصحية
- Markets
- ميانمار (بورما), سنغافورة, تايلاند
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
- sanctions-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- web-presence-since (green), checked 2026-08-05 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-05 Mail server of the company domain
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)