CA 125 ANTIGEN - ANVISA Registration 10345160319

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 10345160319 and manufactured by manufacturer not specified. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA with validity until Mar 28, 2028.

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.

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10345160319
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Registration Details
ANVISA Registration Number: 10345160319
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Related Devices (2)

ADVIA CENTAUR CA 125 II
Risk Class III

Registration Details

10345160319

25351224725200211

01449930000190

Company Information

Dates and Status

Mar 28, 2003

28/03/2028

09/18/2025 19:00:01

ADVIA CENTAUR CA 125 II
Risk Class III

Registration Details

10345160319

25351224725200211

01449930000190

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 28, 2003

28/03/2028

09/18/2025 19:00:01