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- Date of registration
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EUDAMED last updated this device on May 11, 2026
B-0694282042195206942820421952B-06942820421952MD300C2(01)06942820421952
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 Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jan 1, 2020 | Still on market |
CN-MF-000005776No 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.