Awp Dent SRL
Awp Dent SRL, manufacturer registered in Târgu Jiu, Romania
Awp Dent SRL is a company entered in the Romanian trade register (ONRC) under registration number J2015000650182, tax identification code 35179945. The register records a registered office in Târgu Jiu, Gorj county, registration on 2015-10-29, 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 4 employees. Pistol Andrei-Nicolae is listed in the register as administrator.
- Type
- brand seeking distribution
- Location
- Târgu Jiu, Romania
- Founded
- 2015
- Categories
- Medical & Healthcare Supplies
- Markets
- Romania
Listed in a source registry
Verified facts
- sanctions-clear (green), checked 2026-08-22 OpenSanctions
- debarment-clear (green), checked 2026-08-22 OpenSanctions
- registry-activity (green), checked 2026-08-19 Oficiul Național al Registrului Comerțului, date deschise (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-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)
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)