urgo ltd
GB-MF-000029696 · United Kingdom · Loughborough
urgo ltd is registered in the European database on medical devices as a manufacturer, with 316 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 316 |
|---|
Authorised representative in the Union: LABORATOIRES URGO.
Devices declared under this manufacturer
- A'Form C1, Thigh LRG open toe bge
- A'Form C1, Thigh SML clsd toe blk
- A'Form C2, Thigh LRG clsd toe blk
- A'Form C2,BK: LRG, Open Toe, Bge
- A'Form C3,BK: XL, Clsd Toe, Bge
- AltiPress Lpack Lge short, white
- AltiPress Lpack SML short, white
- AltiPress Lpack XXL LNG, beige
- Class 2IISoft BeigeAxilla - MittenRegular
- Class 2IVSoft BeigeBelow KneeRegularClosed Toe
- Class 2IVSoft BeigeTightsRegularOpen Toe
- Class 2VBlackBelow KneeRegularClosed Toe
Showing 12 of 316 declared devices.
Catalogue references include 192391, 558023, 558039, 558226, 558265, 558796.
European nomenclature codes declared: M030405, M030499, M0304010102, M0304010101, M0304010103, M01020202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 316 |
| 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 | 316 |
|---|---|
| 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. urgo ltd was not found in either the U.S. or the Canadian register.