TROPONIN - ANVISA Registration 10347320386
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 10347320386 and manufactured by HORIBA INSTRUMENTS BRASIL LTDA. The registration is held by HORIBA INSTRUMENTS BRASIL LTDA with validity until Jun 23, 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
10347320386
25351018218202528
01759236000179
Company Information
Dates and Status
Jun 23, 2025
23/06/2035
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
FIA Troponina HS
GOLD ANALISA DIAGNOSTICA LTDA
80022230297
Jul 14, 2025

