GeneFirst Limited
GB-MF-000025181 · United Kingdom · Abingdon
GeneFirst Limited is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: Papilloplex.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- Papilloplex HR HPV Genotyping Kit
- Papilloplex® HR-HPV DNA Kit
- Papilloplex® HR-HPV mRNA Kit
- Respiratory 1 Panel
- Respiratory 3 Panel
Catalogue references include MPAHPV001, MPAHPV004, MPAHPV006, RESP003, RESP005.
European nomenclature codes declared: W0105041002, W0105070599.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. GeneFirst Limited was not found in either the U.S. or the Canadian register.