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ANVISA registration 80638720209Valid until Mar 02, 2032

CORONAVIRUS

ANVISA Registration Number: 80638720209DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - MEGUANGZHOU WONDFO BIOTECH CO., LTDRisk Class III
Verified
Device names
Technical name
CORONAVIRUS
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PT: CORONAVÍRUS
Commercial name
COVID-19 AG NASAL RAPID TEST
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Risk class
Class III
Registration details
Registration Number
80638720209
Process Number
25351903239202117
CNPJ
11462456000190
Company information
Registration Holder
DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME
Manufacturer
GUANGZHOU WONDFO BIOTECH CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Mar 02, 2022
Validity
02/03/2032
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 80638720209 and manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Mar 02, 2032.

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.