LEISHMANIA SP - ANVISA Registration 82149920105

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 82149920105 and manufactured by CERTEST BIOTEC, S.L.. The registration is held by GENESTAR INOVAÇÕES E EQUIPAMENTOS MÉDICOS LTDA with validity until Feb 17, 2035.

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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82149920105
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Registration Details
ANVISA Registration Number: 82149920105
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

VIASURE Leishmania Real Time PCR Detection Kit
Risk Class III

Registration Details

82149920105

25351362774202458

35489323000175

Company Information

Spain
PT: ESPANHA

Dates and Status

Feb 17, 2025

17/02/2035

09/18/2025 19:00:01

VIASURE Leishmania Real Time PCR Detection Kit
Risk Class III

Registration Details

82149920105

25351362774202458

35489323000175

Company Information

Dates and Status

Feb 17, 2025

17/02/2035

09/18/2025 19:00:01