Vacsax Limited
GB-MF-000003621 · United Kingdom · Plymouth
Vacsax Limited is registered in the European database on medical devices as a manufacturer, with 149 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 149 |
|---|
Most frequent device types declared: VAL-201.
Authorised representative in the Union: Fannin Ltd..
Devices declared under this manufacturer
- Bacticlear
- Bacticlear ward
- Fluid Guard
- Fluid guard
- Fumevax
- Gelsax Bacticlear
- Gelsax bacticlear
- LAERDAL PUMP ADAPTER KIT
- VACSAX
- Vacsax
- Vommax
- vacsax
Showing 12 of 149 declared devices.
Catalogue references include 3833-188, 9120-008, 9310-341, 9640-008, 9910-040, 9910-358.
European nomenclature codes declared: A06030401, A060399, A06030499, A0680, V9099, Z12011085.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | VACSAX LIMITED (GB) · FDA 3003485902 |
| Devices in EUDAMED | 149 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 149 |
|---|---|
| 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: United States only. Vacsax Limited is registered in the United States but was not found in the Canadian register.