Гуп Лнр "Поз
No description from the company. The catalog line you may see elsewhere is generated by us from the category and location, not a statement by the company.
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Manufacturer (manufacturing registered as the company's activity in the state register; production site not independently confirmed); the register records manufacturing as the company's declared activity (32.50: Производство медицинских инструментов и оборудования), a declaration to the register, not an observation of a working plant
- Location
- Lugansk, Russia
- Founded
- 2022 (from our catalogue record; not confirmed by the company or by a state register)
- Categories
- Suministros médicos y sanitarios
- Markets
- Rusia
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 6 official records from 4 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
- 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. effective since 2026-09-11. EGRUL/EGRIP, Russian state company and sole-trader register (Federal Tax Service)
- Line of business as recorded in the state register: Производство медицинских инструментов и оборудования (record type: registry-activity) [official record; status green] Line of business as recorded in the state register: OKVED2 32.50. Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-09-17. EGRUL/EGRIP, Russian state company and sole-trader register (Federal Tax Service), official extract
- Named directors on file (record type: directors-on-file) [official record; status green] One director named in the company register. The register names the people who run the company, so there is someone answerable if something goes wrong. checked 2026-09-11. EGRUL/EGRIP, Russian state company and sole-trader register (Federal Tax Service)
- Revenue on public record: 184894000 (accounts for 2025) (record type: financials-published) [official record; status green] Annual accounts filed for 2025, revenue RUB 184.9M. Lets you size the supplier against your own volume: the figure comes from accounts filed with the state, not from a claim on a website. checked 2026-10-03. State information resource of accounting statements (FNS), Russia
- Street address on file in the state register (record type: registered-address) [official record; status green] Registered address: 291016, ЛУГАНСКАЯ НАРОДНАЯ, ЛУГАНСК, ФРУНЗЕ, 111А. The address the company itself gave the register, so post and inspectors reach it there. checked 2026-10-03. State information resource of accounting statements (FNS), Russia
- Places goods on the market (national producer register) (record type: places-goods-on-market; this record does not by itself establish manufacturing) [official record; status green] A state register lists this company as placing these goods on the market, as their maker or importer. By itself it does not show who makes them. checked 2026-10-04. Chestny Znak, Russian register of participants in the goods marking system
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.
Recorded in a source
- 1 more officer(s), not named in the record: Head of the company. EGRUL/EGRIP, Russian state company and sole-trader register (Federal Tax Service)
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.