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.
खुदरा फार्मेसी ग्राहकों को सेवा प्रदान करने वाला व्यापक स्वास्थ्य देखभाल उत्पाद और दवा वितरक
कासा मार्ज़म एस.ए. डे सी.वी. स्वास्थ्य आपूर्ति, दवा वितरण और उपभोक्ता कल्याण वस्तुओं को ट्रैक करता है। व्यवसाय निजी चिकित्सा संचालन और सुपरमार्केट के लिए अनुकूलित आपूर्ति समाधान प्रदान करता है। उनकी वितरण वास्तुकला परिवहन चक्रों के दौरान सटीक तापमान नियंत्रण सुनिश्चित करती है।
- 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
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, व्यक्तिगत देखभाल
- Markets
- मैक्सिको
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: चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ (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 व्यक्तिगत देखभाल: 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.