CA 125 ANTIGEN - ANVISA Registration 81246986897

Access comprehensive regulatory information for CA 125 ANTIGEN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81246986897 and manufactured by manufacturer not specified. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until Jun 17, 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 ABBOTT GMBH, 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 Similar Products
5 Competitors
81246986897
2 Related Devices
Registration Details
ANVISA Registration Number: 81246986897
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 VITROS Immunodiagnostic Products CA 125 Reagent Pack and Calibrator
Risk Class III

Registration Details

81246986897

25351037864202411

21921393000146

Dates and Status

Jun 17, 2024

17/06/2034

09/18/2025 19:00:01

Família VITROS Immunodiagnostic Products CA 125 Reagent Pack and Calibrator
Risk Class III

Registration Details

81246986897

25351037864202411

21921393000146

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Jun 17, 2024

17/06/2034

09/18/2025 19:00:01