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ANVISA registration 10033121100Valid until May 18, 2036

TOXOPLASMA GONDII

ANVISA Registration Number: 10033121100BECKMAN COULTER DO BRASIL COMÉRCIO E IMPORTAÇÃO DE PRODUTOS DE LABORATÓRIO LTDABECKMAN COULTER INCRisk Class IV
Verified
Device names
Technical name
TOXOPLASMA GONDII
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Commercial name
Família de Reagente, Calibradores e Controles Access Toxo IgM II
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Risk class
Class IV
Registration details
Registration Number
10033121100
Process Number
25351040079202608
CNPJ
42160812000144
Company information
Registration Holder
BECKMAN COULTER DO BRASIL COMÉRCIO E IMPORTAÇÃO DE PRODUTOS DE LABORATÓRIO LTDA
Manufacturer
BECKMAN COULTER INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
May 18, 2026
Validity
18/05/2036
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 10033121100 and manufactured by BECKMAN COULTER INC. The registration is held by BECKMAN COULTER DO BRASIL COMÉRCIO E IMPORTAÇÃO DE PRODUTOS DE LABORATÓRIO LTDA with validity until May 18, 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.