ANVISA registration
Fixador do fio guia SPE1-Y
Registration 80022069036. Dispositivo Para Fixacao de Cateter
Registration details
| Registration number | 80022069036 |
|---|---|
| Application number | 25351323288202414 |
| Technical name | Dispositivo Para Fixacao de Cateter |
| Risk class | II |
| Published on | 17/06/2024 |
| Validity | Indefinite validity |
Registration holder
| Legal name | FUJIFILM DO BRASIL LTDA |
|---|---|
| CNPJ | 60.397.874/0001-56 |
Manufacturer
- FUJIFILM MEDWORK GMBH ALEMANHA
Other registrations held by FUJIFILM DO BRASIL LTDAview all
IMPRESSORA DE IMAGENS LASER A SECO FUJI DRYPIX 4000
80022060005Phantom-Programa de Controle de Qualidade de Radiografia
80022060006IMPRESSORA A SECO FUJI MEDICAL DRYPIX 7000
80022060012LEITORA DE IMAGEM FCR PRIMA T2
80022060015Chassis Fujifilm
80022060017LEITOR DE IMAGEM FCR PRIMA CR-IR 391 RU
80022060021Source: 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