EUDAMED last updated this device on Sep 8, 2026
VCM502F
59017804VCM502FL2On the marketClass I
- Applicable legislation
- —
- Organization name
- mdh sp. z o. o.
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 →- 05901780432706
- Reference / catalog number
- VCM502F
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.
VCM502F is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by mdh sp. z o. o.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.