EUDAMED last updated this device on Jun 30, 2026
Wearever
081006584HDL600SEOn the marketClass I
- Applicable legislation
- —
- Organization name
- Prime Life Fibers Inc.
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 →- 00810065846235
- Reference / catalog number
- HDL600BLK2X
Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.
Wearever is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Prime Life Fibers Inc.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.