EUDAMED last updated this device on Aug 11, 2026
ALTOSPLINT
88093240410267U4On the marketClass I
- Applicable legislation
- —
- Organization name
- Altochem Co.,Ltd.
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 →- 08809324043432
- Reference / catalog number
- AS500RFW
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.
ALTOSPLINT is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Altochem Co.,Ltd.. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.