ANVISA registration
HI-TORQUE CROSS-IT GUIDE WIRE
Registration 80146501496. FIO GUIA CARDIOVASCULAR
Registration details
| Registration number | 80146501496 |
|---|---|
| Application number | 25351464585200718 |
| Technical name | FIO GUIA CARDIOVASCULAR |
| Risk class | IV |
| Published on | 24/12/2007 |
| Validity | Valid until 24/12/2027 |
Registration holder
| Legal name | ABBOTT LABORATORIOS DO BRASIL LTDA |
|---|---|
| CNPJ | 56.998.701/0001-16 |
Manufacturer
- ABBOTT MEDICAL ESTADOS UNIDOS DA AMÉRICA
Other registrations held by ABBOTT LABORATORIOS DO BRASIL 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