Casa Marzam SA de CV
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 sản phẩm chăm sóc sức khỏe và thuốc toàn diện phục vụ khách hàng nhà thuốc bán lẻ
Casa Marzam S.A. de C.V. xử lý các hoạt động cung cấp dịch vụ y tế, theo dõi việc phân phối dược phẩm và các mặt hàng chăm sóc sức khỏe người tiêu dùng. Doanh nghiệp cung cấp các giải pháp cung ứng tối ưu cho hoạt động y tế tư nhân và siêu thị. Kiến trúc phân phối của chúng đảm bảo kiểm soát nhiệt độ chính xác trong chu kỳ vận chuyển.
- 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
- Mexico City, Mexico
- Founded
- 1934 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- marzam.com.mx
- Categories
- Vật tư y tế và chăm sóc sức khỏe, Chăm sóc cá nhân
- Markets
- Mexico
What is established and what is not
No researcher review has been written for this company yet. 2 official records from 2 official sources are on file. 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
- 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)
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-09-10. GLEIF Global LEI record
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
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)
Goods family established: Vật tư y tế và chăm sóc sức khỏe (the company's own text). The exact product, operation and trade route needed to determine a product-specific requirement are not established here. Product-specific import rules not established for the catalog category Chăm sóc cá nhân: no record or company text names goods of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.
Check independently
Before a first order, ask whose products they sell and on what basis: a distribution agreement or the manufacturer's authorisation.