EUDAMED last updated this device on Jul 27, 2026
AFIAS Testosterone
880613300519CHOn the marketIVDR Class B
- Applicable legislation
- —
- Organization name
- Boditech Med 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 →- 08806133040997
- Reference / catalog number
- SMFP-29
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.
AFIAS Testosterone is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class B. Manufactured by Boditech Med Inc.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.