ANTI-SMOOTH MUSCLE ANTIBODY - ANVISA Registration 80016880009
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 80016880009 and manufactured by DTS - DIAGNOSTIC & TECHNICAL SERVICES CC. The registration is held by NEWLEAF MEDICAMENTOS E DIAGNOSTICO 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
80016880009
25351271123201030
03476756000108
Company Information
Dates and Status
Nov 03, 2010
VIGENTE
09/18/2025 19:00:01
ANTICORPO ANTI-MÚSCULO LISO
iFlash-SMA IgG
SHENZHEN YHLO BIOTECH CO., LTD.
80867150104
Jul 15, 2021
ANTICORPO ANTI-MÚSCULO LISO
Anti-GP2 IgA
GA GENERIC ASSAYS GMBH
80464810549
Nov 06, 2017
ANTICORPO ANTI-MÚSCULO LISO
AESKUSLIDES EMA IgA
AESKU DIAGNOSTICS GMBH & CO. KG
10259610170
Sep 21, 2015
ANTICORPO ANTI-MÚSCULO LISO
AESKUSLIDES EMA IgG
AESKU DIAGNOSTICS GMBH & CO. KG
10259610164
Jun 22, 2015
ANTICORPO ANTI-MÚSCULO LISO
Quanta Lite Actina IgG Elisa
INOVA DIAGNOSTICS, INC.
80003610392
Jun 20, 2014

