Alliance Pharmaceuticals Limited
GB-MF-000023165 · United Kingdom · Chippenham
Alliance Pharmaceuticals Limited is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 27 |
|---|
Most frequent device types declared: 5036631ABSORBGL8001RY, 5036631ALOCTGL800625, 5036631KELOCTSHET8039CY, 5036631LIFTPLSSCT8026U5, 5036631LIFTPLSSP8027Q8.
Authorised representative in the Union: Alliance Pharma (Ireland) Ltd.
Devices declared under this manufacturer
- Aloclair Gél na detské ďasná
- Aloclair Teething Gel
- Alovex Dentizione
- Anaftin Baby Gel gingival
- Anaftin Baby Igemegeel
- Anaftin Baby fogínygél
- Anaftin Baby gelis dygstant dantukams
- KELO-COTE Scar Sheet Body
- Kelo-Cote Scar Sheets C - Section
- Vamousse® Head Lice Treatment Mousse
- opus stoma care absorbagel odour neutralising sachets for ostomy pouch
- opus stoma care liftplus citrus medical adhesive remover non sting spr
Showing 12 of 27 declared devices.
Catalogue references include 5502, 5503, 5504, 5505, 5506, 5507.
European nomenclature codes declared: Q019007, A108005, V901001, M04040702, A108099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| Country of registration | United Kingdom |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 27 |
|---|---|
| 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. Alliance Pharmaceuticals Limited was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
ECM24MDR004 | supplemented | 2029-06-09 |