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ANTINUCLEAR ANTIBODY (ANA) - ANVISA Registration 80003610488

Access comprehensive regulatory information for ANTINUCLEAR ANTIBODY (ANA) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80003610488 and manufactured by INOVA DIAGNOSTICS, INC .. The registration is held by WERFEN MEDICAL 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 INOVA DIAGNOSTICS, INC., ORGENTEC DIAGNOSTIKA GMBH, 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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80003610488
Registration Details
ANVISA Registration Number: 80003610488
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Device Details

QUANTA Flash® CTD Screen Plus Controles
Risk Class II

Registration Details

80003610488

25351003091201510

02004662000165

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 23, 2015

VIGENTE

09/18/2025 19:00:01