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EUDAMED last updated this device on May 12, 2026
6970392211XM000287Fingertip Pulse Oximeter is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by JOYTECH Healthcare Co., Ltd.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
069422846108796970392211XM000287XM-111(01)06942284610879
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z1203020408PULSE OXIMETERS1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | May 12, 2026 | Apr 27, 2027 |
| Germany | May 12, 2026 | Apr 27, 2027 |
CN-MF-000006020No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.6970392211MT00076FOn the marketAmabi6970392211MT00076FOn the marketArm-Type Fully Automatic Blood Pressure Monitor6970392211BP0001Y5On the marketArm-Type Fully Automatic Blood Pressure Monitor6970392211BP0001Y5On the marketArm-Type Fully Automatic Blood Pressure Monitor6970392211BP0002Y7On the market