- Role
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- Date of registration
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EUDAMED last updated this device on May 20, 2026
697022925GCE5XXE606970229251863697022925GCE5XXE6608.13(01)06970229251863
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.
Z12040299GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - OTHER1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 17 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Still on market | |
| Czechia | Still on market | |
| Denmark | Still on market | |
| Spain | Still on market | |
| Finland | Still on market | |
| France | Still on market | |
| Croatia | Still on market | |
| Hungary | Still on market | |
| Italy | Still on market | |
| Netherlands | Still on market | |
| Poland | Still on market | |
| Romania | Still on market | |
| Sweden | Still on market | |
| Slovakia | Still on market | |
| Türkiye | Still on market |
CN-MF-000033595No 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.697022925GCE8XXEMOn the marketCompressor Nebulizer Prolife PN Basic697022925GCE8XXEMOn the marketCOMPRESSOR NEBULIZER Prolife PN Compact697022925GCE8XXEMOn the marketDigital Blood Pressure Monitor Prolife PC2 Basic697022925GCE6XXEBOn the marketDigital Blood Pressure Monitor Prolife PC2 Basic AD697022925GCE6XXEBOn the market