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Medical device registration with ANVISA
Search by number, product, registration holder or CNPJ. The data comes from ANVISA's open data publications and is updated here daily.
Registrations held by LABTEST DIAGNOSTICA S/Aremove
281 registrations
| Product | Registration holder | Class | Validity |
|---|---|---|---|
| Cortisol Reagent Kit10009010495 | LABTEST DIAGNOSTICA S/A | II | Valid |
| Vercentra CP-610009010497 | LABTEST DIAGNOSTICA S/A | II | Valid |
| 17-a- Hydroxyprogesterone Reagent Kit10009010499 | LABTEST DIAGNOSTICA S/A | II | Valid |
| G6PD Reagent Kit (CLIA)10009010500 | LABTEST DIAGNOSTICA S/A | II | Valid |
| Trigger Flex Solution10009010502 | LABTEST DIAGNOSTICA S/A | I | Valid |
| Família Fe Liquiform10009010510 | LABTEST DIAGNOSTICA S/A | II | Valid |
Source: ANVISA open data, medical device file. The database provides registration validity, rather than registration status: a registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.
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HSC manages medical device registration with ANVISA, from risk classification to monitoring the application.
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