Ворсменский завод медицинского инструмента
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.
Firmamız tıbbın her alanına yönelik yeniden kullanılabilir tıbbi aletler üretmektedir. Ürün yelpazesinde tıbbi hemostatik kelepçeler, cerrahi ve damar makasları, anatomik ve cerrahi cımbızlar, neşterler ve amputasyon bıçakları, adenotomlar, spekulum ve kulak spekulumları, laringeal ve nazofaringeal spekulumlar, jinekolojik muayene ve ameliyat aynaları bulunur.
- 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
- Russia
- Website
- xn--b1akdp.xn--p1ai
- Categories
- Tıbbi ve Sağlık Malzemeleri
- Markets
- Rusya
What is established and what is not
No researcher review has been written for this company yet. No official record is 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
- Business email on the company's own domain (record type: corporate-mail-on-domain) [our own observation, not an official record; status green] Shows the domain runs its own email rather than a free mailbox. It describes the domain, not who owns it. checked 2026-08-10. Mail server of the company domain
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.