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EUDAMED last updated this device on May 25, 2026
697081942iBreeze25STAV2Positive Airway Pressure System (PAP System) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Resvent Medical Technology Co., Ltd.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06970819423397697081942iBreeze25STAV2iBreeze Tech(01)06970819423397
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