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ANDROSTENEDIONE - ANVISA Registration 10337680159

Access comprehensive regulatory information for ANDROSTENEDIONE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10337680159 and manufactured by IMMUNOTECH A.S.. The registration is held by GENESE PRODUTOS DIAGNOSTICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including DIAMETRA S.R.L., SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED, 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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10337680159
Registration Details
ANVISA Registration Number: 10337680159
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Device Details

ANDROSTENEDIONA - RIE
Risk Class II

Registration Details

10337680159

25351324235201049

68384155000102

Company Information

IMMUNOTECH A.S.
Czech Republic
PT: TCHECA, REPรšBLICA

Dates and Status

Aug 16, 2010

VIGENTE

09/18/2025 19:00:01