ANTICYTOPLASMIC ANTIBODY - ANVISA Registration 82910510003

Access comprehensive regulatory information for ANTICYTOPLASMIC ANTIBODY in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82910510003 and manufactured by AESKU DIAGNOSTICS GMBH & CO. KG. The registration is held by NACH BRASIL PRODUTOS DIAGNOSTICOS 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 ORGENTEC DIAGNOSTIKA GMBH, INOVA DIAGNOSTICS, INC., 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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82910510003
Registration Details
ANVISA Registration Number: 82910510003
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

AESKUSLIDES ANCA Ethanol
Risk Class II

Registration Details

82910510003

25351035748202531

50161001000196

Company Information

Germany
PT: ALEMANHA

Dates and Status

Apr 28, 2025

VIGENTE

09/18/2025 19:00:01