ANDROSTENEDIONE - ANVISA Registration 80213250474

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 80213250474 and manufactured by ADALTIS. The registration is held by PHAREBEE DIAGNOSTICOS COMERCIO IMPORTACAO E EXPORTACAO DE PRODUTOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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80213250474
Registration Details
ANVISA Registration Number: 80213250474
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Kit de Calibradores Androstenediona Eclectica
Risk Class II

Registration Details

80213250474

25351010039201225

64128853000196

Company Information

ADALTIS
Italy
PT: ITÁLIA

Dates and Status

Mar 26, 2012

VIGENTE

09/18/2025 19:00:01