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EUDAMED last updated this device on May 23, 2026
69344401PF-10AW9DVibeat is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Shenzhen Viatom Technology Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0693444010387569344401PF-10AW9DPF-10AW(01)06934440103875
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 Germany; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Italy | Still on market | |
| XI | Still on market |
CN-MF-000012182No 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.