QUIES SAS
FR-MF-000009589 · France · PALAISEAU
QUIES SAS is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|
Most frequent device types declared: AS001, AS002, AS003, AS004, HC001.
Devices declared under this manufacturer
- Anti Snoring Lozenges C
- Anti Snoring Lozenges HL
- Anti Snoring Nasal Spray
- Anti Snoring Nasal Strips L
- Anti Snoring Nasal Strips SM
- Anti Snoring Oral Spray
- Blister Doculyse
- Blister Docuspray
- Doculyse
- Docuspray
Showing 12 of 13 declared devices.
Catalogue references include 141000W, 141101, 143130, 151100, 154103, 156100.
European nomenclature codes declared: Q03010299, Q03040299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 13 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. QUIES SAS was not found in either the U.S. or the Canadian register.