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ANVISA registration 10298910178Valid until Dec 26, 2033

TOXOPLASMA GONDII

ANVISA Registration Number: 10298910178REVVITY DO BRASIL LTDAWALLAC OYRisk Class IV
Verified
Device names
Technical name
TOXOPLASMA GONDII
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Commercial name
GSP® Neonatal Anti-Toxoplasma IgM Kit
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Risk class
Class IV
Registration details
Registration Number
10298910178
Process Number
25351522647202333
CNPJ
00351210000124
Company information
Registration Holder
REVVITY DO BRASIL LTDA
Manufacturer
WALLAC OY
Manufacturing Country
Finland
PT: FINLÂNDIA
Dates and status
Publication Date
Dec 26, 2023
Validity
26/12/2033
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 10298910178 and manufactured by WALLAC OY. The registration is held by REVVITY DO BRASIL LTDA with validity until Dec 26, 2033.

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.