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ANVISA registration 80537410158Valid until Mar 02, 2036

DENGUE

ANVISA Registration Number: 80537410158CELER BIOTECNOLOGIA S/AGUANGZHOU WONDFO BIOTECH CO. LTDRisk Class III
Verified
Device names
Technical name
DENGUE
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Commercial name
CELER FINECARE DENGUE NS1 TESTE QUALITATIVO
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Risk class
Class III
Registration details
Registration Number
80537410158
Process Number
25351129079202567
CNPJ
04846613000103
Company information
Registration Holder
CELER BIOTECNOLOGIA S/A
Manufacturer
GUANGZHOU WONDFO BIOTECH CO. LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Mar 02, 2026
Validity
02/03/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for DENGUE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80537410158 and manufactured by GUANGZHOU WONDFO BIOTECH CO. LTD. The registration is held by CELER BIOTECNOLOGIA S/A with validity until Mar 02, 2036.

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.