PROSTATE-SPECIFIC ANTIGEN (PSA) - ANVISA Registration 10071770842

Access comprehensive regulatory information for PROSTATE-SPECIFIC ANTIGEN (PSA) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10071770842 and manufactured by manufacturer not specified. The registration is held by ABBOTT DIAGNOSTICOS RAPIDOS S.A. with validity until Nov 30, 2035.

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 SIEMENS HEALTHCARE DIAGNOSTICS INC., ABBOTT IRELAND DIAGNOSTIC DIVISION, 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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10071770842
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Registration Details
ANVISA Registration Number: 10071770842
Janaina dos Santos de Miranda

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Related Devices (2)

PSA Prostate Specific Antigen Semi-Quantitative Ultra Rapid Test Device (Sangue Total/Soro/Plasma)
Risk Class III

Registration Details

10071770842

25351788819201408

50248780000161

Company Information

Dates and Status

Mar 30, 2015

30/11/2035

09/18/2025 19:00:01

PSA Prostate Specific Antigen Semi-Quantitative Ultra Rapid Test Device (Sangue Total/Soro/Plasma)
Risk Class III

Registration Details

10071770842

25351788819201408

50248780000161

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Mar 30, 2015

30/11/2035

09/18/2025 19:00:01