TROPONIN - ANVISA Registration 10298910173
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 10298910173 and manufactured by manufacturer not specified. The registration is held by REVVITY DO BRASIL LTDA with validity until Mar 27, 2033.
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
10298910173
25351455474202250
00351210000124
Company Information
Dates and Status
Mar 27, 2023
27/03/2033
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

