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.
Device Details
Registration Details
80003610392
25351198160201481
02004662000165
Company Information
Dates and Status
Jun 20, 2014
VIGENTE
09/18/2025 19:00:01
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80867150104
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GA GENERIC ASSAYS GMBH
80464810549
Nov 06, 2017
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AESKU DIAGNOSTICS GMBH & CO. KG
10259610170
Sep 21, 2015
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AESKUSLIDES EMA IgG
AESKU DIAGNOSTICS GMBH & CO. KG
10259610164
Jun 22, 2015
ANTICORPO ANTI-MÚSCULO LISO
ENDOMYSIAL TEST KIT (distal oesophagus)
DTS - DIAGNOSTIC & TECHNICAL SERVICES CC
80016880009
Nov 03, 2010

