ANVISA registration
EBD EASYTEST 2019-nCoV Antigen Test (Lateral Flow Method)
Registration 82206010002. CORONAVÍRUS
Registration details
| Registration number | 82206010002 |
|---|---|
| Application number | 25351302722202261 |
| Technical name | CORONAVÍRUS |
| Risk class | III |
| Published on | 23/05/2022 |
| Validity | Valid until 23/05/2032 |
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
Other registrations held by EBD BIOTECH IMPORTACAO E COMERCIO DE PRODUTOS MEDICOS HOSPITALARES LTDAview all
EBD EASYTEST 2019-nCoV Saliva/Sputum Test
82206010001Famíília 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
82206010006EBD Dengue NS1 Antigen Whole Blood/Serum/Plasma Test
82206010007Source: 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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