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ANVISA registration 80474870108Valid until Aug 30, 2032

TOXOPLASMA GONDII

ANVISA Registration Number: 80474870108BIOSUL PRODUTOS DIAGNOSTICOS LTDA - MEHANGZHOU ALLTEST BIOTECH CO., LTDRisk Class IV
Verified
Device names
Technical name
TOXOPLASMA GONDII
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Commercial name
Toxo IgG/IgM
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Risk class
Class IV
Registration details
Registration Number
80474870108
Process Number
25351511742202221
CNPJ
05905525000190
Company information
Registration Holder
BIOSUL PRODUTOS DIAGNOSTICOS LTDA - ME
Manufacturer
HANGZHOU ALLTEST BIOTECH CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Aug 30, 2022
Validity
30/08/2032
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for TOXOPLASMA GONDII in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80474870108 and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD. The registration is held by BIOSUL PRODUTOS DIAGNOSTICOS LTDA - ME with validity until Aug 30, 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.