EUDAMED last updated this device on Aug 20, 2026
Dexcom Clarity
038627CLARITY48- Applicable legislation
- —
- Organization name
- Dexcom
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →- 00386270000705
- Reference / catalog number
- 350-0013
Dexcom Clarity is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Dexcom. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.