EUDAMED last updated this device on Jul 1, 2026
RX-1301
697816810SupportN4On the marketClass I
- Applicable legislation
- —
- Organization name
- Zhenjiang R&X Technology 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 →- 06978168100228
- Reference / catalog number
- RX-1301
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.
RX-1301 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Zhenjiang R&X Technology Co., Ltd.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.