SCHISTOSOMA SP - ANVISA Registration 81148560026
Access comprehensive regulatory information for SCHISTOSOMA SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81148560026 and manufactured by EUROIMMUN AG. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until Aug 29, 2026.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including EUROIMMUN AG, NOVATEC IMMUNDIAGNOSTICA GMBH, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

Janaina dos Santos de Miranda
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Registration Details
81148560026
25351968960201665
93741726000166
Company Information
Dates and Status
Aug 29, 2016
29/08/2026
09/18/2025 19:00:01
SCHISTOSOMA SP
IF: Schistosoma mansoni IgG
EUROIMMUN AG
81148560025
Aug 29, 2016
SCHISTOSOMA SP
IF: Schistosoma mansoni IgG
Not specified
81148560025
Aug 29, 2016
SCHISTOSOMA SP
Anti-Schistosoma mansoni IgM
Not specified
81148560070
Jun 25, 2018
SCHISTOSOMA SP
Anti-Schistosoma mansoni IgM
EUROIMMUN AG
81148560070
Jun 25, 2018
SCHISTOSOMA SP
Anti-Schistosoma mansoni IgG
Not specified
10338930196
Oct 29, 2018
SCHISTOSOMA SP
Kit IBMP Biomol Esquistossomose
INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ
80780040024
May 19, 2025
SCHISTOSOMA SP
Anti-Schistosoma mansoni IgG
EUROIMMUN AG
10338930196
Oct 29, 2018
SCHISTOSOMA SP
Anti-Schistosoma mansoni IgG
Not specified
10338930196
Oct 29, 2018
SCHISTOSOMA SP
NovaLisa® Schistosoma mansoni IgM ELISA
Not specified
80464810601
Sep 24, 2018
SCHISTOSOMA SP
NovaLisa® Schistosoma mansoni IgM ELISA
NOVATEC IMMUNDIAGNOSTICA GMBH
80464810601
Sep 24, 2018