Mekophar
越南药品和医疗产品制造商。
Mekophar 在胡志明市生产药物配方和保健产品。该公司供应药房、医院和经销商渠道。
- Type
- Manufacturer
- Location
- Ho Chi Minh City, Vietnam
- Website
- mekophar.com
- Categories
- 医疗保健用品
- Markets
- 越南, 美国, 日本
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-09 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)