ANVISA registration
HIV 1/2/O Tri-line Human Immunodeficiency Virus Rapid Test Device (Sangue Total/Soro/Plasma)
Registration 10071770815. ANTICORPO DO VIRUS DA IMUNODEFICIÊNCIA HUMANA ADQUIRIDA TIPO 1, TIPO 2 E TIPO 1 SUBGRUPO O (HIV)
Registration details
| Registration number | 10071770815 |
|---|---|
| Application number | 25351788484201451 |
| Technical name | ANTICORPO DO VIRUS DA IMUNODEFICIÊNCIA HUMANA ADQUIRIDA TIPO 1, TIPO 2 E TIPO 1 SUBGRUPO O (HIV) |
| Risk class | IV |
| Published on | 30/03/2015 |
| Validity | Valid until 31/05/2036 |
Registration holder
| Legal name | ABBOTT DIAGNOSTICOS RAPIDOS S.A. |
|---|---|
| CNPJ | 50.248.780/0001-61 |
Manufacturer
- ABON BIOPHARM (HANGZHOU) CO LTD CHINA, REPÚBLICA POPULAR
Other registrations held by ABBOTT DIAGNOSTICOS RAPIDOS S.A.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.
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