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EUDAMED last updated this device on Nov 21, 2025
5060693520389WYTEAM3I NB3 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by ArjoHuntleigh AB. Placed on the EU market in Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
050519680353255060693520389WYTEAM3I NB3(01)05051968035325
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.
Z12080101FOETAL MONITORSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Ireland; available across 15 countries total.
| Country | On market since | Until |
|---|---|---|
| IrelandPrimary placement | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Denmark | Still on market | |
| Spain | Still on market | |
| Finland | Still on market | |
| France | Still on market | |
| Italy | Still on market | |
| Netherlands | Still on market | |
| Norway | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Sweden | Still on market | |
| Türkiye | Still on market | |
| XI | Still on market |
SE-MF-000000696No 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.