Welland Medical Ltd
GB-MF-000033194 · United Kingdom · Crawley
Welland Medical Ltd is registered in the European database on medical devices as a manufacturer, with 5 901 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 901 |
|---|
Most frequent device types declared: Aura, Aura Plus, Aurum, Aurum Plus, Belt.
Among these devices, 4 are declared active.
Authorised representative in the Union: Advena Limited.
Catalogue references include 1U1G23S-3-GB1, X1C1A11S-30-PL2, XBLTL01-1-CA2, XMH2NF535-5-NL1, XMHCL513-30-CR1, XMHCS513-30-AU2.
European nomenclature codes declared: A100199, A100302, A108001, A100299, M04041503, A0699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 901 |
| 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 | 5 901 |
|---|---|
| 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. Welland Medical Ltd was not found in either the U.S. or the Canadian register.