TROPONIN - ANVISA Registration 81246986843
Access comprehensive regulatory information for TROPONIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81246986843 and manufactured by ORTHO-CLINICAL DIAGNOSTICS. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until Aug 26, 2029.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ROCHE DIAGNOSTICS GMBH, BODITECH MED INC., 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.
Related Devices (2)
Registration Details
81246986843
25351304030201951
21921393000146
Company Information
Dates and Status
Aug 26, 2019
26/08/2029
09/18/2025 19:00:01
TROPONINA
BIOCLIN POCT FIA TROPONINA I
QUIBASA QUÍMICA BÁSICA LTDA
10269360479
Sep 15, 2025
TROPONINA
Luminis FIA Troponina I
Not specified
80474870163
Sep 08, 2025
TROPONINA
Luminis FIA Troponina I
QINGDAO HIGHTOP BIOTECH CO.,LTD.
80474870163
Sep 08, 2025
TROPONINA
BIOCLIN POCT FIA TROPONINA I-US
QUIBASA QUÍMICA BÁSICA LTDA
10269360475
Aug 04, 2025
TROPONINA
FIA Troponina HS
GOLD ANALISA DIAGNOSTICA LTDA
80022230297
Jul 14, 2025

