IVD SOFTWARE - ANVISA Registration 80254180464

Access comprehensive regulatory information for IVD SOFTWARE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180464 and manufactured by manufacturer not specified. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Mar 11, 2034.

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 ROCHE DIAGNOSTICS GMBH, BIOARRAY SOLUTIONS LTD., 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
80254180464
2 Related Devices
Registration Details
ANVISA Registration Number: 80254180464
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)

BRAHMS Fast Screen Pre I Plus
Risk Class III

Registration Details

80254180464

25351068482202421

04930429000139

Company Information

Dates and Status

Mar 11, 2024

11/03/2034

09/18/2025 19:00:01

BRAHMS Fast Screen Pre I Plus
Risk Class III

Registration Details

80254180464

25351068482202421

04930429000139

Company Information

B-R-A-H-M-S GMBH
Germany
PT: ALEMANHA

Dates and Status

Mar 11, 2024

11/03/2034

09/18/2025 19:00:01