Adg Dent SRL
Adg Dent SRL, manufacturer registered in Cluj-Napoca, Romania
Adg Dent SRL is a company entered in the Romanian trade register (ONRC) under registration number J2016000024122, tax identification code 35377047. The register records a registered office in Cluj-Napoca, Cluj county, registration on 2016-01-06, the legal form SRL and the status funcțiune (in operation). The principal activity reported in the company's annual financial statement filed with the Ministry of Finance for 2025 is CAEN 3250, manufacture of medical and dental instruments and supplies. The same filing reports an average of 9 employees. Ghirișan Darius Teodor is listed in the register as administrator.
- Type
- brand seeking distribution
- Location
- Cluj-Napoca, Romania
- Founded
- 2016
- Categories
- 医療およびヘルスケア用品
- Markets
- ルーマニア
Listed in a source registry
Verified facts
- sanctions-clear (green), checked 2026-08-22 OpenSanctions
- debarment-clear (green), checked 2026-08-22 OpenSanctions
- registry-id-verified (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- workforce-on-record (green), checked 2026-08-19 Ministerul Finanțelor, situații financiare anuale (data.gov.ro)
- leadership-on-record (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- registered-address (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- registered-since (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- registry-active-global (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
- registry-activity (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (data.gov.ro)
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)