ANVISA registration
Fio Guia para Procedimentos Endoscópicos
Registration 10334789014. FIO GUIA DE USO GERAL, NÃO VASCULAR
Registration details
| Registration number | 10334789014 |
|---|---|
| Application number | 25351084671202522 |
| Technical name | FIO GUIA DE USO GERAL, NÃO VASCULAR |
| Risk class | II |
| Published on | 02/06/2025 |
| Validity | Indefinite validity |
Registration holder
| Legal name | G.F.E. DO BRASIL LTDA. |
|---|---|
| CNPJ | 55.126.981/0001-00 |
Manufacturer
- G-FLEX EUROPE SRL BÉLGICA
Other registrations held by G.F.E. DO BRASIL LTDA.view 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