Spectromatch Ltd
GB-MF-000009147 · United Kingdom · Bath
Spectromatch Ltd is registered in the European database on medical devices as a manufacturer, with 186 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 186 |
|---|
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- DS5 - Derma-sil Silicone Gum 5 Shore 1.1kg
- DSPT - Derma-sil Silicone Catalyst 0.5kg
- DSPT - Derma-sil Silicone Catalyst 1kg
- QWAL - QuickWeigh LSR Aubergine 50g
- QWDML - QuickWeigh LSR Deep Mottle 10g
- QWDML - QuickWeigh LSR Deep Mottle 50g
- QWORL - QuickWeigh LSR Orange 200g
- QWPL - QuickWeigh LSR Pink 10g
- RS12 M5 - Reality Series M511 1.2 125g
- RS21 DS - Reality Series Dermasil 2.1 50g
- RS31 M5 - Reality Series M511 3.1 50g
- RS34 DS - Reality Series Dermasil 3.4 50g
Showing 12 of 186 declared devices.
Catalogue references include DS5-1.1, DSPT-1, QWDML-10, QWPL-10, RS21 DS40-50, RS31 M5-50.
European nomenclature codes declared: Y0699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 186 |
| 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 | 186 |
|---|---|
| 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. Spectromatch Ltd was not found in either the U.S. or the Canadian register.