Haleon Medical Devices
IE-MF-000002458 · Ireland · Co.Waterford
Haleon Medical Devices is registered in the European database on medical devices as a manufacturer, with 221 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 221 |
|---|
Devices declared under this manufacturer
- PARODONTAX Complete Protection Blancheur
- PARODONTAX Protection Fluor
- PARODONTAX Réparation Intense Gencives Blancheur & Éclat
- Parodontax Complete Protection Extra Fresh
- Parodontax Herbal Fresh
- SENSODYNE Clinical Repair LIMPIEZA PROFUNDA
- SENSODYNE Clinical Réparateur Nettoyage Intense
- SENSODYNE Clinical Réparateur Éclat Blancheur
- SENSODYNE Répare & Protège Menthe
- Sensodyne Rapid Relief Whitening
- Sensodyne Repair & Protect
- Sensodyne Repair & Protect Mint
Showing 12 of 221 declared devices.
Catalogue references include A1K0000000UJ014, A1K0000000UJ016, A1K0000000W1003, A1K0000000X1002, A1K0000000XD009, A1K0000000XD018.
European nomenclature codes declared: Q0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 221 |
| Country of registration | Ireland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 221 |
|---|---|
| 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. Haleon Medical Devices was not found in either the U.S. or the Canadian register.