Chronolab Systems, S.L.
ES-MF-000017043 · Spain · Sant Climent de Llobregat
Chronolab Systems, S.L. is registered in the European database on medical devices as a manufacturer, with 154 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- ASO, R1 1 x 45 mL, R2 1 x 5 mL, CAL 1 x 1 mL
- Albumin, 3 x 100 mL
- Bilirubin Total, 8 x 100 mL
- Infectious mononucleosis, 50 tests
- Magnesium, 2 x 100 mL
- Protein in urine & CSF
- Proteus OX19, 20 x 5 mL
- Proteus OX2, 20 x 5 mL
- RF Latex, 1 x 5 mL
- Rheumatoid factor (RF), 5 mL Latex, 1 mL Positive control, 1 mL Negati
- Salmonella Paratyphi BO, 1 x 5 mL
- Salmonella Typhi H, 20 x 5 mL
Showing 12 of 154 declared devices.
Catalogue references include 101-0062, 101-0191, 101-0218, 101-0236, 101-0248, 101-0599.
European nomenclature codes declared: W0105011002, W0105011712, W01010205, W01010204, W01010203, W0105011701.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 154 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Chronolab Systems, S.L. was not found in either the U.S. or the Canadian register.