HELICOBACTER PYLORI - ANVISA Registration 80002670069

Access comprehensive regulatory information for HELICOBACTER PYLORI in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80002670069 and manufactured by RENYLAB QUÍMICA E FARMACÊUTICA LTDA. The registration is held by RENYLAB QUÍMICA E FARMACÊUTICA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including VEDALAB, MONOBIND, 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 Similar Products
5 Competitors
80002670069
Registration Details
ANVISA Registration Number: 80002670069
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

URETEST
Risk Class II

Registration Details

80002670069

25351674829201099

00562583000144

Company Information

Brazil
PT: BRASIL

Dates and Status

Dec 20, 2010

VIGENTE

09/18/2025 19:00:01