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

TRIIODOTHYRONINE (T3) - ANVISA Registration 82102680003

Access comprehensive regulatory information for TRIIODOTHYRONINE (T3) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82102680003 and manufactured by GUANGZHOU BIOSURPASS BIOTECHNOLOGY CO., LTD. The registration is held by Diagnóstica Indústria e Comércio LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ADALTIS S.R.L., ROCHE DIAGNOSTICS GMBH, 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
82102680003
Registration Details
ANVISA Registration Number: 82102680003
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

T3 FIA Analyzer Test
Risk Class II

Registration Details

82102680003

25351139029202598

11462456000270

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 15, 2025

VIGENTE

09/18/2025 19:00:01