ANVISA registration
EBD Dengue NS1 Antigen Whole Blood/Serum/Plasma Test
Registration 82206010007. DENGUE
Registration details
| Registration number | 82206010007 |
|---|---|
| Application number | 25351494999202219 |
| Technical name | DENGUE |
| Risk class | III |
| Published on | 02/01/2023 |
| Validity | Valid until 02/01/2033 |
Registration holder
| Legal name | EBD BIOTECH IMPORTACAO E COMERCIO DE PRODUTOS MEDICOS HOSPITALARES LTDA |
|---|---|
| CNPJ | 13.977.106/0001-91 |
Manufacturer
- GUANGZHOU WONDFO BIOTECH CO. LTD CHINA, REPÚBLICA POPULAR
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82206010002Famíília de Frascos de Hemocultura Automatizados EBD
82206010003Sistemas de Hemocultura Automáticos EBD BACT
82206010004EBD EASY COVID AG AUTOTEST
82206010005EBD EASYTEST Troponin I Whole Blood/Serum/Plasma Test
82206010006Source: 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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