CliniMed Limited
GB-MF-000023784 · United Kingdom · Loudwater
CliniMed Limited is registered in the European database on medical devices as a manufacturer, with 62 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 62 |
|---|
Among these devices, 14 are declared sterile.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- Appeel® Adhesive Remover (non-sterile)
- CliniFix® Universal Hydrocolloid Securement Device
- CliniPeel® Medical Adhesive Remover Wipes
- CliniSure Urinary Sheath Standard 24mm
- CliniSure Urinary Sheath Standard 35mm - Sample
- CliniSure Urinary Sheath Wide band 24mm
- CliniSure Urinary Sheath Wide band 40mm
- LBF Barrier Cream, 100g
- LBF Barrier Cream, 2g
- LBF Barrier Cream, 30g
- LBF® Sterile Barrier Film Foam Applicator 1ml
- LBF® Sterile No Sting Barrier Film Spray 30ml
Showing 12 of 62 declared devices.
Catalogue references include 3500, 3510-20, 3824, 3826, 3831, 3900.
European nomenclature codes declared: U070201, A108005, M04010203, M0202010102, M9002, M04040901.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 62 |
| 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 | 62 |
|---|---|
| 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. CliniMed Limited was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
GB23/00000102 | issued | 2028-02-27 |