Medibord Limited
UK-MF-000038315 · United Kingdom · Derby
Medibord Limited is registered in the European database on medical devices as a manufacturer, with 64 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 64 |
|---|
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- Avior P1
- Avior P1c
- Kuma V
- Libra 1
- MED-Indexing
- Medibord
- Mirak S2
- Mirak S3
- Nova D
- Nova R
- Nova S
- Vega
Showing 12 of 64 declared devices.
Catalogue references include CAAE-01B, PHIN70-AC, PHINCXS-AC, SBMR-HN, SBV450-IB, SSMR-TC2.
European nomenclature codes declared: V0804.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 64 |
| 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 | 64 |
|---|---|
| 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. Medibord Limited was not found in either the U.S. or the Canadian register.