- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 25, 2026
697081942iBreeze25STAV206970819423380697081942iBreeze25STAV2iBreeze 30STA Pro(01)06970819423380
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.
Z12030102CONTINUOUS POSITIVE PRESSURE EQUIPMENT1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Spain; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Still on market | |
| Türkiye | Still on market |
CN-MF-000012608No 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.697081942HR02KQOn the marketPositive Airway Pressure System (PAP System)697081942iBreeze20CZ5On the marketPositive Airway Pressure System (PAP System)697081942iBreeze20CZ5On the marketPositive Airway Pressure System (PAP System)697081942iBreeze25STAV2On the marketPositive Airway Pressure System (PAP System)697081942iBreeze25STAV2On the market