- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 12, 2026
697204011AOJ30X17FArm Blood Pressure Monitor is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Shenzhen AOJ Medical Technology Co., Ltd.. Placed on the EU market in Czechia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06972040117595697204011AOJ30X17FARM-30G2(01)06972040117595
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.
Z1203020501NON–INVASIVE OSCILLOMETRIC BLOOD PRESSURE GAUGES1 warning recorded — scroll inside the panel to see all entries.
CW011No certificate specifically references this device's Basic UDI-DI.
Primary placement in Czechia; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| CzechiaPrimary placement | Jun 12, 2026 | Jun 11, 2029 |
| Hungary | Jun 12, 2026 | Jun 11, 2029 |
| Poland | Jun 12, 2026 | Jun 11, 2029 |
| Slovakia | Jun 12, 2026 | Jun 11, 2029 |
CN-MF-000018386No 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.