D-DIMER - ANVISA Registration 80102513412

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 80102513412 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 22, 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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80102513412
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Registration Details
ANVISA Registration Number: 80102513412
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família AutoLumo D-Dímero Micropartículas (CLIA)
Risk Class III

Registration Details

80102513412

25351455434202470

04718143000194

Dates and Status

Apr 22, 2025

22/04/2035

09/18/2025 19:00:01

Família AutoLumo D-Dímero Micropartículas (CLIA)
Risk Class III

Registration Details

80102513412

25351455434202470

04718143000194

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 22, 2025

22/04/2035

09/18/2025 19:00:01