Kazakhstan Pharmaceutical Company MedService LLP
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.
Производитель дженериков, инфузионных растворов и медицинского оборудования для больниц.
ТОО «МедСервис» управляет сертифицированным GMP фармацевтическим заводом в Алматы, производящим таблетки, инъекционные препараты, инфузии и одноразовые шприцы. Компания обеспечивает государственные программы здравоохранения, больничные сети и экспортирует продукцию в республики Центральной Азии.
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Almaty, Kazakhstan
- Founded
- 2005 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- https://www.medservice.kz
- Categories
- Медицинские товары и расходники
What is established and what is not
No researcher review has been written for this company yet. No fact of any kind is on file either. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Relationships
1 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Candidates, not confirmed
- medservice.kz: Website of this business. Source 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)
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.