Griffiths and Nielsen
GB-MF-000016341 · United Kingdom · Horsham
Griffiths and Nielsen is registered in the European database on medical devices as a manufacturer, with 38 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 38 |
|---|
Most frequent device types declared: Anti Embolism Stocking, Fitlegs EverydayLife, Fitlegs Sport, Illuminated proctoscope.
Among these devices, 3 are declared active.
Authorised representative in the Union: CS Life Sciences Europe Ltd.
Devices declared under this manufacturer
- Fitlegs AES
- Fitlegs EverydayLife
- Fitlegs Sport
- Proctolux
- Proctolux 19mm
- Sigmolux
Showing 12 of 38 declared devices.
Catalogue references include 402001, 402004, 403002, 451002, 451006, 454000.
European nomenclature codes declared: M030405, G06.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | GRIFFITHS AND NIELSEN MEDICAL (GB) · FDA 3008808122 |
| Devices in EUDAMED | 38 |
| Country of registration | United Kingdom |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 38 |
|---|---|
| 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.