CORONAVIRUS - ANVISA Registration 10355870401

Access comprehensive regulatory information for CORONAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10355870401 and manufactured by HIBERGENE DIAGNOSTICS. The registration is held by BIOMÉDICA EQUIPAMENTOS E SUPRIMENTOS HOSPITALARES LTDA with validity until Mar 29, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including GUANGZHOU WONDFO BIOTECH CO., LTD., Eco Diagnostica Ltda, 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
10355870401
2 Related Devices
Registration Details
ANVISA Registration Number: 10355870401
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

Related Devices (2)

Família Kit HiberGene COVID-19
Risk Class III

Registration Details

10355870401

25351647172202044

01299509000140

Company Information

Ireland
PT: IRLANDA

Dates and Status

Mar 29, 2021

29/03/2031

09/18/2025 19:00:01

Família Kit HiberGene COVID-19
Risk Class III

Registration Details

10355870401

25351647172202044

01299509000140

Company Information

Dates and Status

Mar 29, 2021

29/03/2031

09/18/2025 19:00:01