Descarpack Descartáveis do Brasil Ltda.
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.
Sản phẩm y tế và bệnh viện dùng một lần
Nhà sản xuất màn, áo choàng, mũ và bao giày phẫu thuật dùng một lần để sử dụng trong bệnh viện. Descarpack sản xuất vật tư y tế tiệt trùng và không tiệt trùng cho ngành chăm sóc sức khỏe Brazil.
- 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
- São Paulo, Brazil
- Founded
- 1991 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- https://www.descarpack.com.br
- Categories
- Vật tư y tế và chăm sóc sức khỏe
- Markets
- Brazil
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. 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
- Active legal entity ID (LEI) (record type: lei-active) [official record; status green] A global identifier used in finance; an active one is renewed yearly. checked 2026-09-07. GLEIF global LEI register (golden copy)
- Website domain registered (record type: domain-registered) [our own observation, not an official record; status green] Shows how long this web address has been registered. That is the age of the domain, not of the company: a domain can change owners. checked 2026-08-27. Domain registry record
- 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
- 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 for the production site address and a document linking that site to this legal entity.