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ANVISA registration 81472060047Valid until Aug 11, 2035

COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III

ANVISA Registration Number: 81472060047ADVAGEN BIOTECH LTDAHANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.Risk Class III
Verified
Device names
Technical name
COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III
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PT: PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III
Commercial name
Teste Rápido COVID-19 e Influenza A + B
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Risk class
Class III
Registration details
Registration Number
81472060047
Process Number
25351071175202517
CNPJ
22565307000172
Company information
Registration Holder
ADVAGEN BIOTECH LTDA
Manufacturer
HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Aug 11, 2025
Validity
11/08/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81472060047 and manufactured by HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.. The registration is held by ADVAGEN BIOTECH LTDA with validity until Aug 11, 2035.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.