Instrument intended for immunoassays - ANVISA Registration 82910510005

Access comprehensive regulatory information for Instrument intended for immunoassays in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82910510005 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 HANGZHOU ALLTEST BIOTECH CO. LTD, ACRO BIOTECH, INC. (MONTCLAIR), 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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82910510005
Registration Details
ANVISA Registration Number: 82910510005
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

HELIOS® AUTOMATED IFA SYSTEM
Risk Class II

Registration Details

82910510005

25351134033202560

50161001000196

Company Information

Germany
PT: ALEMANHA

Dates and Status

Sep 15, 2025

VIGENTE

09/18/2025 19:00:01