D-DIMER - ANVISA Registration 80146501907

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 80146501907 and manufactured by BIOKIT SA. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until Dec 22, 2034.

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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80146501907
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Registration Details
ANVISA Registration Number: 80146501907
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Quantia D-Dimer Control
Risk Class III

Registration Details

80146501907

25351588437201483

56998701000116

Company Information

BIOKIT SA
Spain
PT: ESPANHA

Dates and Status

Dec 22, 2014

22/12/2034

09/18/2025 19:00:01

Quantia D-Dimer Control
Risk Class III

Registration Details

80146501907

25351588437201483

56998701000116

Company Information

Dates and Status

Dec 22, 2014

22/12/2034

09/18/2025 19:00:01