Endocarts International Limited
GB-MF-000004309 · United Kingdom · Essex
Endocarts International Limited is registered in the European database on medical devices as a manufacturer, with 61 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 61 |
|---|
Authorised representative in the Union: Acorn Regulatory Consultancy Services Ltd.
Devices declared under this manufacturer
- AES-1
- AES-5
- EC-55 Monitor Cart
- Endotrans 10 tray cart (no tray)
- Endotrans 6 tray cart (no tray)
- FF-5 Cart with Transformer
- MIG-10 LITE
- MIG-20
- MIG-20 Cart with Transformer
- S/N-2 Lens
- VC-2010ENT
- VC-2010HF
Showing 12 of 61 declared devices.
Catalogue references include 101248, 101286, 101315, 101420, 103344, 103626EC.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 61 |
| 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 | 61 |
|---|---|
| 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. Endocarts International Limited was not found in either the U.S. or the Canadian register.