- Role
- Country
- Date of registration
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EUDAMED last updated this device on Feb 13, 2025
506106630TGARW5KSK-MF-000045565No 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.3 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW038Primary placement in Netherlands; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Feb 13, 2025 | Still on market |
| Austria | Feb 13, 2025 | Still on market |
| Czechia | Feb 13, 2025 | Still on market |
| Germany | Feb 13, 2025 | Still on market |
| Denmark | Feb 13, 2025 | Still on market |
| Norway | Feb 13, 2025 | Still on market |
| Poland | Feb 13, 2025 | Still on market |
| Portugal | Feb 13, 2025 | Still on market |
| Sweden | Feb 13, 2025 | Still on market |
| Slovakia | Feb 13, 2025 | Still on market |
| XI | Feb 13, 2025 | Still on market |
(01)05061066300027
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.
A108005DEVICES FOR THE REMOVAL OF ADHESIVES FROM THE PERISTOMAL SKIN