D-DIMER - ANVISA Registration 10246810349

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 10246810349 and manufactured by WIENER LABORATORIOS S.A.I.C.. The registration is held by LABORLAB PRODUTOS PARA LABORATÓRIOS LTDA EPP with validity until Aug 07, 2033.

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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10246810349
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Registration Details
ANVISA Registration Number: 10246810349
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família D-Dimer Turbitest AA
Risk Class III

Registration Details

10246810349

25351191779202317

72807043000194

Company Information

Argentina
PT: ARGENTINA

Dates and Status

Aug 07, 2023

07/08/2033

09/18/2025 19:00:01

Família D-Dimer Turbitest AA
Risk Class III

Registration Details

10246810349

25351191779202317

72807043000194

Company Information

Dates and Status

Aug 07, 2023

07/08/2033

09/18/2025 19:00:01