ANVISA registration
Material de Moldagem Auricular
Registration 80179150082. Material de moldagem auricular
Registration details
| Registration number | 80179150082 |
|---|---|
| Application number | 25351720023201901 |
| Technical name | Material de moldagem auricular |
| Risk class | I |
| Published on | 26/12/2019 |
| Validity | Indefinite validity |
Registration holder
| Legal name | STARKEY DO BRASIL LTDA |
|---|---|
| CNPJ | 04.216.059/0001-72 |
Manufacturer
- DREVE-OTOPLASTIK GMBH ALEMANHA
Other registrations held by STARKEY DO BRASIL LTDAview all
APARELHO DIGITAL PARA SURDEZ RETROAURICULAR
80179150066Aparelho Digital para Surdez Retroauricular
80179150068Aparelho Digital para Surdez Retroauricular
80179150069APARELHO DIGITAL PARA SURDEZ RETROAURICULAR
80179150070Aparelho Digital para Surdez Retroauricular
80179150071Aparelho Digital para Surdez Intra Auricular (ITE), Intra Canal (ITC), Microcanal (CIC)
80179150074Source: 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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