Rapid Labs Ltd
GB-MF-000026335 · United Kingdom · Colchester, Essex
Rapid Labs Ltd is registered in the European database on medical devices as a manufacturer, with 51 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: Analyzer, Monoclonal, Reader.
Among these devices, 1 are declared sterile.
Authorised representative in the Union: VidaQuick Biotech S.L..
Devices declared under this manufacturer
- Anti-B Monoclonal
- Anti-D (IgG & IgM) Monoclonal
- CA15-3 Rapid Test Device – WB/S/P
- Campylobacter Rapid Test Device – Feces
- Cardiac Troponin T Rapid Test Device – WB/S/P
- Cup Reader
- Enterovirus 71 Ag Test Device-Feces
- Etomidate (ETO) Rapid Test Device-Saliva
- Ketamine (KET) Rapid Test Panel
- Marijuana (THC) Rapid Test Panel
- Marijuana (THC) Rapid Test Strip
- Morphine (MOP) Rapid Test Strip
Showing 12 of 51 declared devices.
Catalogue references include BG-B10, BG-D10, D-CAMD10, D-DOA73D20S, D-DOA9P40, D-FIEV71AGD10.
European nomenclature codes declared: W0102160599, W0201020201, W02010701, W0103030101, W0105040602, W0102090299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 51 |
| 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 | Licensed in Canada |
|---|---|
| Matched entry | RAPID LABS LIMITED |
North American profile: Canada only. Rapid Labs Ltd holds a Canadian licence but was not found in the U.S. register.