EUDAMED last updated this device on Sep 23, 2026
PURATU
B-08682054131385On the marketClass IIb
- Applicable legislation
- —
- Organization name
- ATILGAN TIBBİ ÜRÜNLER SAĞLIK HİZMETLERİ ANONİM ŞİRKETİ
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 →- 08682054131385
- Reference / catalog number
- TNARS.TI.70
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.
PURATU is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by ATILGAN TIBBİ ÜRÜNLER SAĞLIK HİZMETLERİ ANONİM ŞİRKETİ. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.