Technovent Limited
GB-MF-000006738 · United Kingdom · Bridgend
Technovent Limited is registered in the European database on medical devices as a manufacturer, with 373 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 373 |
|---|
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- Extrinsic Colouring Kit
- Factor II Skin Shade Warm Brown , 30ml
- Intrinsic Master Colour Kit
- LSR Silicone Elastomer (2Ib Kit)
- Maxi Insert Keeper S-Range
- Maxi Magnacap for Medicon Basic Post S-Range
- Maxi O-Ring Magnet S-Range
- Realistic Silicone (1Ib Kit)-12 Shore
- Softening Agent (25g)
- Technovent Dry Pigment Purple (7g)
- Technovent Dry Pigment Umber (7g)
- Technovent Flocking Pink 50g
Showing 12 of 373 declared devices.
Catalogue references include A-588-1, FI-SK23, M513 (25), P-MC2-S, P199, P217.
European nomenclature codes declared: Y0699, A108008, Q0299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | TECHNOVENT LIMITED (GB) · FDA 9617078 |
| Devices in EUDAMED | 373 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 373 |
|---|---|
| Found in the U.S. device database | 90 |
| Share | 24.1 % |
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: United States only. Technovent Limited is registered in the United States but was not found in the Canadian register.