Stafford-Miller (Ireland) Limited
IE-MF-000002788 · Ireland · Dungarvan, Co. Waterford
Stafford-Miller (Ireland) Limited is registered in the European database on medical devices as a manufacturer, with 80 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 61 |
|---|---|
| Class IIb | 19 |
Devices declared under this manufacturer
- COREGA EXTRA STRONG
- COREGA Super Strong Mild Mint
- Corega BIO Tabs
- Corega Bio Formula
- Corega Blanqueador
- Corega Max Czyszczenie
- Corega Power Max MAX UPEVNENIE + SVIEŽOSŤ
- Corega Power Max Ultimate All in 1
- Corega Super Strong Flavour Free
- Corega Supreme
- Corega Ultra
- Corega Ultra Fresh
Showing 12 of 80 declared devices.
Catalogue references include A1K0000000PE005, A1K0000000Q2005, A1K0000000Q5005, A1K0000000TZ002, A1K0000000XO001, A1K0000000XR018.
European nomenclature codes declared: Q010280, D99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 80 |
| 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 | 80 |
|---|---|
| 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. Stafford-Miller (Ireland) Limited was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
GB23/00000413 | issued | 2028-12-08 |