Ardo medical AG
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- Type
- brand seeking distribution
- Location
- Unterägeri, Switzerland
- Website
- https://ardo.ch
- Categories
- Fournitures médicales et de santé
- Markets
- Suisse
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-22 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-22 OpenSanctions
- debarment-clear (green), checked 2026-08-22 OpenSanctions
- registry-active-global (green), checked 2026-08-22 Zefix (Swiss commercial registry)
- fda-registered (green), checked 2026-08-22 FDA
- lei-lapsed (amber), checked 2026-08-22 GLEIF
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)