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ANVISA registration 81124120031Valid until Jun 18, 2030

CORONAVIRUS

ANVISA Registration Number: 81124120031MOLECULAR BIOTECNOLOGIA LTDAXIAMEN BOSON BIOTECH CO., LTDRisk Class III
Verified
Device names
Technical name
CORONAVIRUS
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PT: CORONAVÍRUS
Commercial name
Rapid 2019-nCoV IgG/IgM Combo Test Card
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Risk class
Class III
Registration details
Registration Number
81124120031
Process Number
25351396896202014
CNPJ
15562934000194
Company information
Registration Holder
MOLECULAR BIOTECNOLOGIA LTDA
Manufacturer
XIAMEN BOSON BIOTECH CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 18, 2020
Validity
18/06/2030
Last Updated
08/18/2026 19:00:00
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 81124120031 and manufactured by XIAMEN BOSON BIOTECH CO., LTD. The registration is held by MOLECULAR BIOTECNOLOGIA LTDA with validity until Jun 18, 2030.

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.