LEISHMANIA SP - ANVISA Registration 80524900058

Access comprehensive regulatory information for LEISHMANIA 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 80524900058 and manufactured by manufacturer not specified. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Jun 12, 2027.

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 VIRCELL S.L., ADVAGEN BIOTECH LTDA, 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.

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80524900058
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Registration Details
ANVISA Registration Number: 80524900058
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

TESTE RÁPIDO ONSITE LEISHIMANIA IGG/IgM Combo
Risk Class III

Registration Details

80524900058

25351098537201706

09593438000103

Company Information

Dates and Status

Jun 12, 2017

12/06/2027

09/18/2025 19:00:01

TESTE RÁPIDO ONSITE LEISHIMANIA IGG/IgM Combo
Risk Class III

Registration Details

80524900058

25351098537201706

09593438000103

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 12, 2017

12/06/2027

09/18/2025 19:00:01