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

CORONAVIRUS - ANVISA Registration 82444370176

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 82444370176 and manufactured by GENESYSTEM CO., LTD.. The registration is held by Enzytec Biotecnologia Ltda. with validity until Jan 27, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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 Competitors
5 Recent Registrations
82444370176
2 Related Devices
Registration Details
ANVISA Registration Number: 82444370176
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

SMARTCHEK® SARS-CoV-2 Detection Kit
Risk Class III

Registration Details

82444370176

25351370066202491

07214566000165

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Jan 27, 2025

27/01/2035

09/18/2025 19:00:01

SMARTCHEK® SARS-CoV-2 Detection Kit
Risk Class III

Registration Details

82444370176

25351370066202491

07214566000165

Company Information

Dates and Status

Jan 27, 2025

27/01/2035

09/18/2025 19:00:01