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.
Distributeur complet de produits de santé et de médicaments au service des clients des pharmacies de détail
Casa Marzam S.A. de C.V. gère l'approvisionnement en soins de santé, suit la distribution pharmaceutique et les articles de bien-être des consommateurs. L'entreprise propose des solutions d'approvisionnement optimisées pour les établissements médicaux privés et les supermarchés. Leur architecture de distribution garantit des contrôles précis de la température pendant les cycles de transport.
- 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
- Fournitures médicales et de santé, Hygiène et soins personnels
- Markets
- Mexique
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: Fournitures médicales et de santé (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 Hygiène et soins personnels: 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.