ANVISA registration 82036180018ActiveCORONAVÍRUS
ANVISA Registration Number: 82036180018CONNECT ASSUNTOS REGULATÓRIOS, COMÉRCIO E DISTRIBUIDORA DE PRODUTOS MÉDICO-HOSPITALRES LTDAHOYOTEK BIOMEDICAL CO., LTDRisk Class III
Device names
- Commercial name
- Corona Virus (COVID-19) Antigen Rapid Test (Colloidal Gold) – Nasopharyngeal swab / Oropharyngeal swab
- Risk class
- Class III
Registration details
- Registration Number
- 82036180018
- Process Number
- 25351357641202117
- CNPJ
- 37026700000165
Company information
- Registration Holder
- CONNECT ASSUNTOS REGULATÓRIOS, COMÉRCIO E DISTRIBUIDORA DE PRODUTOS MÉDICO-HOSPITALRES LTDA
- Manufacturer
- HOYOTEK BIOMEDICAL CO., LTD
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- Mar 21, 2022
- Status
- Active
About this record
Access comprehensive regulatory information for CORONAVÍRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82036180018 and manufactured by HOYOTEK BIOMEDICAL CO., LTD. The registration is held by CONNECT ASSUNTOS REGULATÓRIOS, COMÉRCIO E DISTRIBUIDORA DE PRODUTOS MÉDICO-HOSPITALRES LTDA with validity until Mar 21, 2032.
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