Farmexim
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
Nhà phân phối dược phẩm tiên phong cung cấp sản phẩm lâm sàng cho mạng lưới y tế toàn quốc
Farmexim cung cấp dịch vụ hậu cần chăm sóc sức khỏe và phân phối dược phẩm chất lượng cao. Công ty quản lý các nhà kho chuyên dụng và một đội xe giao hàng được kiểm soát nhiệt độ. Họ phục vụ hàng ngàn hiệu thuốc và phòng khám y tế trên khắp Romania.
- Type
- Not established by any record (our catalog import lists it as distributor; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Bucharest, Romania
- Founded
- 1990 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- farmexim.ro
- Categories
- Vật tư y tế và chăm sóc sức khỏe
- Markets
- Romania
What is established and what is not
No researcher review has been written for this company yet. 1 official record from 1 official source is on file. 1 other entry is not an official record: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Certificates named on their own site (record type: certificate-page-on-site; this record does not by itself establish manufacturing) [stated or published by the company, not an official record; status amber] Shows where the company itself claims the certificate, so you can open that page and judge it. checked 2026-09-18. Company's own certification page
- Legal entity ID lapsed (record type: lei-lapsed) [official record; status amber] The global finance identifier was not renewed. checked 2026-09-07. GLEIF global LEI register (golden copy)
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)
Check independently
Before a first order, ask whose products they sell and on what basis: a distribution agreement or the manufacturer's authorisation.