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ANTI-SMOOTH MUSCLE ANTIBODY - ANVISA Registration 80003610392

Access comprehensive regulatory information for ANTI-SMOOTH MUSCLE 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 80003610392 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 AESKU DIAGNOSTICS GMBH & CO. KG, SCIMEDX CORPORATION, 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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80003610392
Registration Details
ANVISA Registration Number: 80003610392
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Device Details

Quanta Lite Actina IgG Elisa
Risk Class II

Registration Details

80003610392

25351198160201481

02004662000165

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 20, 2014

VIGENTE

09/18/2025 19:00:01