CooperVision Manufacturing Limited
GB-MF-000021104 · United Kingdom · Southampton
CooperVision Manufacturing Limited is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 11 |
|---|
Among these devices, 11 are declared sterile.
Authorised representative in the Union: CooperVision CL Kft..
Catalogue references include many.
European nomenclature codes declared: Q021004010101, Q0210040102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | COOPERVISION MANUFACTURING, LTD. (GB) · FDA 3003981983 |
| Devices in EUDAMED | 11 |
| Country of registration | United Kingdom |
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. CooperVision Manufacturing Limited is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G10 103773 0009 | issued | 2030-03-13 |