EUDAMED last updated this device on Sep 9, 2026
Pulse Oximeter
B-06945040109877On the marketClass IIb
- Applicable legislation
- —
- Organization name
- Contec Medical Systems 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 →- 06945040109877
- Reference / catalog number
- PO-200A Solo
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.
Pulse Oximeter is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Contec Medical Systems Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.