Tody Laboratories Int. SRL
RO-MF-000032726 · Romania · Bucharest
Tody Laboratories Int. SRL is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: 50S.
Devices declared under this manufacturer
- ADENOVIRUS RAPID TEST CASSETTE (FECES)
- AFP RAPID TEST CASSETTE (WHOLE BLOOD/SERUM/PLASMA)
- CEA RAPID TEST CASSETTE (WHOLE BLOOD/SERUM/PLASMA)
- ROTAVIRUS RAPID TEST CASSETTE (FECES)
- TSH RAPID TEST CASSETTE (WHOLE BLOOD/SERUM/PLASMA)
- URINE STRIPS READER - 50S
- URINE STRIPS READER - S300
Catalogue references include C20US1001, C20US1005, C61RT1001, C61RT1005, C61RT1022, C61RT1027.
European nomenclature codes declared: W02010701, W01020410, W0105040606, W0102039001, W0102030112, W0105040601.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| Country of registration | Romania |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| 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. Tody Laboratories Int. SRL was not found in either the U.S. or the Canadian register.