Dental Shop Orimed
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.
Dental Shop Orimed - PL merkezli üretici
Dental Shop Orimed, Króla Zygmunta Augusta 9, 08-445 Osieck, Polonya'da bulunan bir üreticidir.
- 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
- Osieck, Poland
- Website
- https://sklep.orimed.pl/pl/
- Categories
- Tıbbi ve Sağlık Malzemeleri, Diş Malzemeleri ve Ekipmanları
- Markets
- Polonya
What is established and what is not
No researcher review has been written for this company yet. 2 official records from 2 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
- Street address on file in the state register (record type: registered-address) [official record; status green] Registered address: KRÓLA ZYGMUNTA AUGUSTA 9, 08-445 OSIECK. The address the company itself gave the register, so post and inspectors reach it there. checked 2026-10-03. Ministry of Finance VAT white list (Poland)
- EU VAT number valid for cross-border trade (record type: vat-valid) [official record; status green] The number is registered and active: we asked the EU VIES service and it answered yes. An invalid VAT number is the first sign an invoice comes from the wrong company. checked 2026-08-01. VIES (European Commission)
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: Diş Malzemeleri ve Ekipmanları (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 category Tıbbi ve Sağlık Malzemeleri: 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 production site address and a document linking that site to this legal entity.