- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Oct 15, 2025
735017801073501780100086ASE-MF-0000481184 warnings recorded — scroll inside the panel to see all entries.
CW275CW135CW011CW999Primary placement in Sweden; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Jun 18, 2025 | Still on market |
| Austria | Still on market | |
| Belgium | Still on market | |
| Bulgaria | Still on market | |
| Cyprus | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Denmark | Still on market | |
| Estonia | Still on market | |
| EL | Still on market | |
| Spain | Still on market | |
| Finland | Still on market | |
| France | Still on market | |
| Croatia | Still on market | |
| Hungary | Still on market | |
| Ireland | Still on market | |
| Iceland | Still on market | |
| Italy | Still on market | |
| Liechtenstein | Still on market | |
| Lithuania | Still on market | |
| Luxembourg | Still on market | |
| Latvia | Still on market | |
| Malta | Still on market | |
| Netherlands | Still on market | |
| Norway | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Romania | Still on market | |
| Slovenia | Still on market | |
| Slovakia | Still on market | |
| Türkiye | Still on market | |
| XI | Still on market |
(01)07350178010008
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.
R060203INHALATION THERAPY HUMIDIFICATION LIQUIDS735017801073501780100466JOn the marketSinaVita® Allergy Support Nasal Spray735017801073501780100536FOn the marketSinaVita® Immune Support Inhalation Drops735017801073501780100846SOn the marketSinaVita® Immune Support Nasal Spray735017801073501780100606COn the marketSinaVita® Immune Support Oral Spray735017801073501780100776VOn the marketNo 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.