ANVISA registration
FIO GUIA PARA IMPLANTES S4 AESCULAP
Registration 80136999045. Fio Guia
Registration details
| Registration number | 80136999045 |
|---|---|
| Application number | 25351603406201455 |
| Technical name | Fio Guia |
| Risk class | II |
| Published on | 15/12/2014 |
| Validity | Indefinite validity |
Registration holder
| Legal name | LABORATORIOS B. BRAUN S/A |
|---|---|
| CNPJ | 31.673.254/0001-02 |
Manufacturer
- AESCULAP AG ALEMANHA
Other registrations held by LABORATORIOS B. BRAUN S/Aview all
PROTETOR DO TRANSDUTOR DE PRESSAO
10008530002PROTESE VASCULAR UNI-GRAFT
10008530004STERIFIX INFUSAO - FILTRO DE INFUSAO DE 0,2 MICRAPARA INFUSAO DE SOLUCOES
10008530021VENOSTRIP FLEBO EXTRATOR
10008530022EXTENSOFIX - EXTENSAO PARA EQUIPO DE INFUSAO PARENTERAL
10008530027PERFUSOR SET - DISPOSITIVO PARA A EXTENSAO DE EQUIPOS
10008530030Source: 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