Abouttoothlife S.R.L.
Abouttoothlife S.R.L., manufacturer registered in Bacău, Romania
Abouttoothlife S.R.L. is a company entered in the Romanian trade register (ONRC) under registration number J4/1421/2022, tax identification code 46660030. The register records a registered office in Bacău, registration on 2022-08-17, 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 2024 is CAEN 3250, manufacture of medical and dental instruments and supplies. The same filing reports an average of 6 employees. Atudorei Constantin is listed in the register as administrator.
- Type
- brand seeking distribution
- Location
- Bacău, Romania
- Founded
- 2022
- Categories
- 医疗保健用品
- Markets
- 罗马尼亚
Listed in a source registry
Verified facts
- sanctions-clear (green), checked 2026-08-23 OpenSanctions
- debarment-clear (green), checked 2026-08-23 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)