Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
10298910173
2 Related Devices
Registration Details
ANVISA Registration Number: 10298910173
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Famรญlia SuperFlex Cardiac Troponin I
Risk Class III

Registration Details

10298910173

25351455474202250

00351210000124

Company Information

Dates and Status

Mar 27, 2023

27/03/2033

09/18/2025 19:00:01

Famรญlia SuperFlex Cardiac Troponin I
Risk Class III

Registration Details

10298910173

25351455474202250

00351210000124

Company Information

China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

Mar 27, 2023

27/03/2033

09/18/2025 19:00:01