D-DIMER - ANVISA Registration 80474870166

Access comprehensive regulatory information for D-DIMER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80474870166 and manufactured by QINGDAO HIGHTOP BIOTECH CO.,LTD.. The registration is held by BIOSUL PRODUTOS DIAGNOSTICOS LTDA - ME with validity until Sep 08, 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 ROCHE DIAGNOSTICS GMBH, INSTRUMENTATION LABORATORY, 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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80474870166
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Registration Details
ANVISA Registration Number: 80474870166
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Luminis FIA D-Dímero
Risk Class III

Registration Details

80474870166

25351098581202519

05905525000190

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 08, 2025

08/09/2035

09/18/2025 19:00:01

Luminis FIA D-Dímero
Risk Class III

Registration Details

80474870166

25351098581202519

05905525000190

Company Information

Dates and Status

Sep 08, 2025

08/09/2035

09/18/2025 19:00:01