FASAJ GROUP
UK-MF-000048354 · United Kingdom · Greater London
FASAJ GROUP is registered in the European database on medical devices as a manufacturer, with 74 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 74 |
|---|
Most frequent device types declared: SKU 1450, SKU 1400, SKU 1425, SKU 1850, SKU 750, SKU 1675\t, SKU 925\t, sku 1600, sku 1800, sku 1925, sku 2005\t\t, sku1975, sku2000, sku2015, sku2020, sku2025, sku2095, sku2100, sku2105.
Authorised representative in the Union: SUNGO Europe B.V..
Catalogue references include sku 1525 Small, sku1100 Medium, sku1575 Large, sku2050 X-Large, sku3000 Large, sku3005 Medium.
European nomenclature codes declared: T04010103, T04010201, V08068002, T04010101, V0812.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 74 |
| 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 | 74 |
|---|---|
| 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. FASAJ GROUP was not found in either the U.S. or the Canadian register.