ТОО "CENTRAL ASIA MEDICAL INDUSTRIES"
- Type
- brand seeking distribution
- Location
- Алматы, Kazakhstan
- Categories
- Perlengkapan Medis & Kesehatan
Listed in a source registry
Kazakhstan, register of domestic manufacturers (e-ondiris.gov.kz)
Verified facts
- registered-manufacturer (green), checked 2026-08-30 Register of domestic manufacturers, Kazakhstan (e-ondiris.gov.kz)
- sanctions-clear (green), checked 2026-08-31 OpenSanctions
- debarment-clear (green), checked 2026-08-31 OpenSanctions
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)