Дезон
The Dezon company presents high-quality disinfectants, professional detergents and cleaning products on the...
The Dezon company presents high-quality disinfectants, professional detergents and cleaning products on the Russian market. All products offered by us have all the necessary certificates. Our products are intended for medical institutions, food and industrial enterprises in Russia. The range of products produced includes about 100 items.
- Type
- Manufacturer
- Location
- Russia
- Website
- dezon.pro
- Categories
- Specialty & Gourmet Food, Medical & Healthcare Supplies, Cleaning & Household Supplies
- Markets
- Russia
Verified facts
- domain-registered (green), checked 2026-08-08 Domain registry record
- registered-address (green), checked 2026-08-20 State information resource of accounting statements (FNS), Russia
- registry-activity (green), checked 2026-08-20 State information resource of accounting statements (FNS), Russia
- financials-published (green), checked 2026-08-19 State information resource of accounting statements (FNS), Russia
- registry-active-global (green), checked 2026-08-19 State information resource of accounting statements (FNS), Russia
- registered-manufacturer (green), checked 2026-08-08 Единый реестр субъектов МСП (ФНС России)
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- tax-debt-clear (green), checked 2026-08-13 Открытые данные ФНС России
- annual-accounts-filed (green), checked 2025-12-31 Открытые данные ФНС России
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)