ANVISA registration
HI-TORQUE SUPRA CORE 35 GUIDE WIRE
Registration 80146501611. FIO GUIA CARDIOVASCULAR
Registration details
| Registration number | 80146501611 |
|---|---|
| Application number | 25351193094200908 |
| Technical name | FIO GUIA CARDIOVASCULAR |
| Risk class | IV |
| Published on | 05/10/2009 |
| Validity | Valid until 05/10/2034 |
Registration holder
| Legal name | ABBOTT LABORATORIOS DO BRASIL LTDA |
|---|---|
| CNPJ | 56.998.701/0001-16 |
Manufacturer
- ABBOTT VASCULAR 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.
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