Beh-Buian
- Type
- Manufacturer
- Location
- Chișinău, Moldova
- Categories
- 医疗保健用品
Listed in a source registry
Verified facts
- registered-since (green), checked 2026-08-22 Registrul de stat al unitatilor de drept (dataset.gov.md)
- registry-id-verified (green), checked 2026-08-22 Registrul de stat al unitatilor de drept (dataset.gov.md)
- debarment-clear (green), checked 2026-08-23 OpenSanctions
- sanctions-clear (green), checked 2026-08-23 OpenSanctions
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)