CAPRIZNAYA MODA
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.
La empresa CAPRIZNAYA MODA produce ropa elegante y moderna para el personal médico. El catálogo de la marca incluye batas, chaquetas, blusas, monos quirúrgicos, pantalones y monos médicos. Los productos están creados para médicos, trabajadores médicos subalternos, cosmetólogos y técnicos de salones de belleza. Las principales direcciones de la empresa: suministro al por mayor de ropa médica, confección de medicina corporativa.
- 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
- capriznayamoda.ru
- Categories
- Tejidos y materiales textiles, Cuidado personal, Suministros médicos y sanitarios
- Markets
- Rusia
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
- First recorded on the web archive (record type: web-presence-since) [our own observation, not an official record; status green] The company website was already online in 2024. Shows a web archive saw a page at this address on that date. It does not show who ran the site then. checked 2026-08-03. Internet Archive (Wayback)
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: Suministros médicos y sanitarios (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 categories Tejidos y materiales textiles, Cuidado personal: 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 for the legal entity's registration number and country, then check it in the official register.