TROPONIN - ANVISA Registration 80022230297
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 80022230297 and manufactured by GOLD ANALISA DIAGNOSTICA LTDA. The registration is held by GOLD ANALISA DIAGNOSTICA LTDA with validity until Jul 14, 2035.
This page provides complete technical specifications for this device, 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.
Device Details
Registration Details
80022230297
25351050929202597
03142794000116
Company Information
Dates and Status
Jul 14, 2025
14/07/2035
09/18/2025 19:00:01
TROPONINA
BIOCLIN POCT FIA TROPONINA I
QUIBASA QUรMICA BรSICA 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 QUรMICA BรSICA LTDA
10269360475
Aug 04, 2025
TROPONINA
Yumizen M Troponina I
HORIBA INSTRUMENTS BRASIL LTDA
10347320386
Jun 23, 2025

