D-DIMER - ANVISA Registration 10287411211

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 10287411211 and manufactured by manufacturer not specified. The registration is held by ROCHE DIAGNÓSTICA BRASIL LTDA with validity until Apr 10, 2027.

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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10287411211
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Registration Details
ANVISA Registration Number: 10287411211
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família D-Dimer Gen.2
Risk Class III

Registration Details

10287411211

25351303402201627

30280358000186

Company Information

Dates and Status

Apr 10, 2017

10/04/2027

09/18/2025 19:00:01

Família D-Dimer Gen.2
Risk Class III

Registration Details

10287411211

25351303402201627

30280358000186

Company Information

Germany
PT: ALEMANHA

Dates and Status

Apr 10, 2017

10/04/2027

09/18/2025 19:00:01