TROPONIN - ANVISA Registration 80474870163
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 80474870163 and manufactured by manufacturer not specified. The registration is held by BIOSUL PRODUTOS DIAGNOSTICOS LTDA - ME with validity until Sep 08, 2035.
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
80474870163
25351098543202566
05905525000190
Company Information
Dates and Status
Sep 08, 2025
08/09/2035
09/18/2025 19:00:01
TROPONINA
BIOCLIN POCT FIA TROPONINA I
QUIBASA QUรMICA BรSICA LTDA
10269360479
Sep 15, 2025
TROPONINA
BIOCLIN POCT FIA TROPONINA I-US
QUIBASA QUรMICA BรSICA LTDA
10269360475
Aug 04, 2025
TROPONINA
FIA Troponina HS
GOLD ANALISA DIAGNOSTICA LTDA
80022230297
Jul 14, 2025
TROPONINA
Yumizen M Troponina I
HORIBA INSTRUMENTS BRASIL LTDA
10347320386
Jun 23, 2025
TROPONINA
Famรญlia Pathonorm Cardiac Acute Liq
Not specified
80117581225
Jun 16, 2025

