Medinox London Limited
GB-MF-000009467 · United Kingdom · London
Medinox London Limited is registered in the European database on medical devices as a manufacturer, with 116 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 116 |
|---|
Most frequent device types declared: MX70101, MX76112.
Authorised representative in the Union: Medinox Health Ireland Limited.
Devices declared under this manufacturer
- MX MX KINESIOLOGY TAPE - BEIGE (5CM X 5M)
- MX MX KINESIOLOGY TAPE - YELLOW (5CM X 5M)
- MX PREMIUM ELASTICATED ANKLE SUPPORT - SMALL
- MX PREMIUM ELASTICATED ELBOW SUPPORT - XLARGE
- MX PREMIUM ELASTICATED KNEE SUPPORT - LARGE
- MX PREMIUM ELASTICATED WRIST SUPPORT - XLARGE
- MX PREMIUM NEOPRENE WRIST SUPPORT AMBI REMOVABLE SPLINTS L/XL/XXL
- MX PREMIUM UNIVERSAL ANKLE SUPPORT - UNI S/M/L
- MX PREMIUM UNIVERSAL DOUBLE PATELLA STRAP UNI S/M/L
- MX STANDARD ELASTICATED ANKLE SUPPORT - XXL
- MX STANDARD ELASTICATED HAND SUPPORT - L
- MX STANDARD ELASTICATED KNEE SUPPORT -L
Showing 12 of 116 declared devices.
Catalogue references include MX71151, MX72131, MX72211, MX74191, MX74201, MX74591.
European nomenclature codes declared: M030402010103, M030402030102, M03040299, M04040301, Y060609, Y06120601.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 116 |
| 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 | 116 |
|---|---|
| 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. Medinox London Limited was not found in either the U.S. or the Canadian register.