EUDAMED last updated this device on Jul 23, 2026
MDFS100
0821925000215BOn the marketClass I
- Applicable legislation
- —
- Organization name
- Gyrus ACMI, 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 →- 00821925027787
- Reference / catalog number
- MDFS100
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.
MDFS100 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Gyrus ACMI, Inc.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.