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EUDAMED last updated this device on May 14, 2026
6970392211XM000287069422846108316970392211XM000287XM-113(01)06942284610831
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 OXIMETERSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Austria; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Dec 1, 2024 | Apr 27, 2027 |
| Belgium | Dec 1, 2024 | Apr 27, 2027 |
| Germany | Dec 1, 2024 | Apr 27, 2027 |
| Spain | Dec 1, 2024 | Apr 27, 2027 |
| France | Dec 1, 2024 | Apr 27, 2027 |
| Hungary | Dec 1, 2024 | Apr 27, 2027 |
| Italy | Dec 1, 2024 | Apr 27, 2027 |
| Netherlands | Dec 1, 2024 | Apr 27, 2027 |
| Poland | Dec 1, 2024 | Apr 27, 2027 |
| Portugal | Dec 1, 2024 | Apr 27, 2027 |
| Sweden | Dec 1, 2024 | 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