ANVISA registration
BIOTEK Dispositivo de reparação de Menisco (All inside)
Registration 81464750165. Kit de Sutura
Registration details
| Registration number | 81464750165 |
|---|---|
| Application number | 25351679023202397 |
| Technical name | Kit de Sutura |
| Risk class | III |
| Published on | 29/10/2024 |
| Validity | Valid until 29/10/2034 |
Registration holder
| Legal name | Domo Salute Consultoria Regulatória Ltda |
|---|---|
| CNPJ | 26.263.959/0001-03 |
Manufacturer
- CHETAN MEDITECH PVT. LTD. ÍNDIA
Other registrations held by Domo Salute Consultoria Regulatória Ltdaview all
Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this 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.
Next step
Medical device registration with ANVISA
HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.
Speak to a specialist