Hemofarm a.d.
Hemofarm quảng cáo sản xuất thuốc gốc cho các kênh B2B sẵn sàng xuất khẩu.
Hemofarm quảng cáo sản xuất thuốc gốc, sản phẩm vô trùng và công thức dược phẩm ở Vrsac. Được thành lập vào năm 1960, công ty cung cấp cho các hiệu thuốc, bệnh viện, nhà phân phối chăm sóc sức khỏe và thị trường xuất khẩu trên khắp RS, BA, MK, DE và các thị trường xuất khẩu liên quan.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Vrsac, Serbia
- Founded
- 1960
- Website
- hemofarm.com
- Categories
- Vật tư y tế và chăm sóc sức khỏe
- Markets
- Serbia, Bosnia và Herzegovina, Bắc Macedonia, Đức
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
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- product-authorised-for-sale (green), checked 2026-08-21 Ministry of Health of Armenia, State Register of Medicinal Products (pharm.am)
- sanctions-clear (green), checked 2026-08-12 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-12 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- domain-registered (green), checked 2026-08-12 Domain registry record
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)