CORONAVIRUS
ANVISA Registration Number: 82036180017CONNECT 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)
- Risk class
- Class III
Registration details
- Registration Number
- 82036180017
- Process Number
- 25351319859202173
- 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
- Nov 16, 2021
- Status
- Active
About this record
Access comprehensive regulatory information for CORONAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82036180017 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 Nov 16, 2031.
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