D-DIMER - ANVISA Registration 80638720182

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 80638720182 and manufactured by manufacturer not specified. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Jun 21, 2031.

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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80638720182
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Registration Details
ANVISA Registration Number: 80638720182
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Risk Class III

Registration Details

80638720182

25351469593202117

11462456000190

Company Information

Dates and Status

Jun 21, 2021

21/06/2031

09/18/2025 19:00:01

D-DÍMERO TEST CASSETE FIA
Risk Class III

Registration Details

80638720182

25351469593202117

11462456000190

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 21, 2021

21/06/2031

09/18/2025 19:00:01