Cryolab Limited
UK-MF-000043881 · United Kingdom · Chichester
Cryolab Limited is registered in the European database on medical devices as a manufacturer, with 26 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 26 |
|---|
Most frequent device types declared: CryoBank Series, CryoCan Series, CryoCrest Series, CryoFill Series, CryoNest® Series.
Among these devices, 6 are declared active, 6 with a measuring function.
Authorised representative in the Union: AQUA - CHEMIE spol. s r.o.
Devices declared under this manufacturer
- CryoBank 1150-55
- CryoBank 800-39
- CryoCan 47-10
- CryoCan 47-6
- CryoCrest 35L
- CryoCrest 50L
- CryoFill 240
- CryoFill 500
- CryoNest® XL
- CryoNest® XXL
- CryoNest® XXXL
- CryoStork® V10
Showing 12 of 26 declared devices.
Catalogue references include CryoBank1150-55, CryoBank800-39, CryoCrest35, CryoFill240, CryoFill500, CryoNestXXL.
European nomenclature codes declared: U08020401, W05030499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 26 |
| 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 | 26 |
|---|---|
| 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. Cryolab Limited was not found in either the U.S. or the Canadian register.