Blumont Healthcare Ltd
GB-MF-000010003 · United Kingdom · Grantham
Blumont Healthcare Ltd is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 17 |
|---|
Most frequent device types declared: ED-1601, ED-1606, EG-1602, EO-1617, EO-1622.
Among these devices, 17 are declared sterile.
Authorised representative in the Union: MedNet EC-REP IIb GmbH.
Devices declared under this manufacturer
- Carbofresh Gel
- Clinitas Gel
- Ocufresh Lubricating Eye Drops
- Ocufresh Lubricating Eye gel
- Ocufresh Night
- Ocufresh-C Lubricating Eye Drops
- Simple Eye Ointment
- Xailin Gel DE
- Xailin Gel EN
- Xailin Hydrate (Samples)
- Xailin Hydrate Eye Drops
- Xailin Night (Samples)
Showing 12 of 17 declared devices.
Catalogue references include 1602A, 1602C, 1602D, 1602E, 1606B, 1617A.
European nomenclature codes declared: Q0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. Blumont Healthcare Ltd was not found in either the U.S. or the Canadian register.