CherryLAB OÜ
- Type
- Manufacturer
- Location
- Saustinõmme küla, Estonia
- Founded
- 2026
- Categories
- 의료 및 건강 관리 용품
Listed in a source registry
Verified facts
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 2026-07-08 e-Äriregister (RIK)
- directors-on-file (green), checked 2026-08-24 e-Äriregister (RIK)
- leadership-on-record (green), checked 2026-07-08 e-Äriregister (RIK)
- ownership-on-record (green), checked 2026-08-24 e-Äriregister (RIK)
- sanctions-clear (green), checked 2026-07-27 OpenSanctions
- debarment-clear (green), checked 2026-07-27 OpenSanctions
- registry-active-global (green), checked 2026-07-27 e-Äriregister
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)