Dita Bělská
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 (32500: 32500), a declaration to the register, not an observation of a working plant
- Location
- Boskovice, Czechia
- Founded
- 2013 (matches the state register)
- Categories
- Perlengkapan Medis & Kesehatan
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 3 official records from 1 official source 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
- Legally registered and still active (record type: registry-active-global) [official record; status red] Indicates the company is not dissolved or winding down. checked 2026-08-24. ARES (Czech business register)
- On the company register (record type: registered-since) [official record; status green] On the company register since 2013-01-09. Shows how long the company has been on the state register, which is hard to fake and easy to check. effective since 2013-01-09. ARES (Czech business register)
- registry-activity (record type: registry-activity) [official record; status green] Activity code in the state register: NACE 32500. Shows what the state itself says the company does, which you can compare with what it promises you. effective since 2013-01-09. ARES (Czech business register)
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.