EUDAMED last updated this device on Aug 5, 2026
J SHAPE CANNULA
B-08681092050252On the marketClass IIa
- Applicable legislation
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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 →- 08681092050252
- Reference / catalog number
- C04-005
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.
J SHAPE CANNULA is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by MMT MERAN MEDİKAL TEKNOLOJİ KOLL. ŞTİ. Ahmet Cemil Baytaş ve Fatma Baytaş. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.