Banzai Lab. S.R.L.
Banzai Lab. S.R.L., manufacturer registered in Constanţa, Romania
Banzai Lab. S.R.L. is a company entered in the Romanian trade register (ONRC) under registration number J2018000805132, tax identification code 39116826. The register records a registered office in Constanţa, registration on 2018-03-30, 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 7 employees. Zamfir Ștefan is listed in the register as administrator.
- Type
- brand seeking distribution
- Location
- Constanţa, Romania
- Founded
- 2018
- Categories
- Tıbbi ve Sağlık Malzemeleri
- Markets
- Romanya
Listed in a source registry
Verified facts
- debarment-clear (green), checked 2026-08-22 OpenSanctions
- sanctions-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)