ADITEK DO BRASIL, SA
- Type
- Manufacturer
- Location
- CRAVINHOS Sao Paulo, Brazil
- Categories
- Dental Supplies & Equipment
Listed in a source registry
Verified facts
- sanctions-clear (green), checked 2026-08-14 OpenSanctions
- debarment-clear (green), checked 2026-08-14 OpenSanctions
- fda-registered (green), checked 2026-08-14 FDA
- lei-active (green), checked 2026-08-14 GLEIF
- registered-manufacturer (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
Claimed certifications
- FDA Registered FDA Establishment Registration
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)