D-DIMER - ANVISA Registration 80020690215

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 80020690215 and manufactured by BIO-RAD LABORATORIES INC. The registration is held by BIO-RAD LABORATORIOS BRASIL LTDA with validity until May 17, 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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80020690215
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Registration Details
ANVISA Registration Number: 80020690215
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Liquichek D-Dimer Control
Risk Class III

Registration Details

80020690215

25351088239201056

03188198000177

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 17, 2010

17/05/2035

09/18/2025 19:00:01

Família Liquichek D-Dimer Control
Risk Class III

Registration Details

80020690215

25351088239201056

03188198000177

Company Information

Dates and Status

May 17, 2010

17/05/2035

09/18/2025 19:00:01