ANVISA registration
Famíília de Frascos de Hemocultura Automatizados EBD
Registration 82206010003. MEIOS DE CULTURA E DISPOSITIVOS DESTINADOS EXCLUSIVAMENTE À SEMEADURA PRIMÁRIA
Registration details
| Registration number | 82206010003 |
|---|---|
| Application number | 25351147636202289 |
| Technical name | MEIOS DE CULTURA E DISPOSITIVOS DESTINADOS EXCLUSIVAMENTE À SEMEADURA PRIMÁRIA |
| Risk class | I |
| Published on | 07/07/2022 |
| Validity | Indefinite validity |
Registration holder
| Legal name | EBD BIOTECH IMPORTACAO E COMERCIO DE PRODUTOS MEDICOS HOSPITALARES LTDA |
|---|---|
| CNPJ | 13.977.106/0001-91 |
Manufacturer
- SCENKER BIOLOGICAL TECHNOLOGY 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
82206010001EBD EASYTEST 2019-nCoV Antigen Test (Lateral Flow Method)
82206010002Sistemas 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.
Next step
Medical device registration with ANVISA
HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.
Speak to a specialist