ANVISA registration
Fio guia hidrofílico esterilizado padrão
Registration 10306840169. FIO GUIA DE USO GERAL, NÃO VASCULAR
Registration details
| Registration number | 10306840169 |
|---|---|
| Application number | 25351667518201997 |
| Technical name | FIO GUIA DE USO GERAL, NÃO VASCULAR |
| Risk class | II |
| Published on | 09/12/2019 |
| Validity | Indefinite validity |
Registration holder
| Legal name | PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA |
|---|---|
| CNPJ | 00.028.682/0001-40 |
Manufacturer
- MICRO-TECH (NANJING) CO., LTD. CHINA, REPÚBLICA POPULAR
Other registrations held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES 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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