EUDAMED last updated this device on Feb 16, 2026
6050771
73955026107115AMZOn the marketClass I
- Applicable legislation
- —
- Organization name
- Mediplast AB
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 →- 07395502097041
- Reference / catalog number
- 6050771
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.
6050771 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Mediplast AB. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.