D-DIMER - ANVISA Registration 80132390013

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 80132390013 and manufactured by Continental produtos biologicos ltda. The registration is held by CONTINENTAL PRODUTOS BIOLOGICOS LTDA with validity until Aug 09, 2031.

This page provides complete technical specifications for this device, 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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80132390013
Registration Details
ANVISA Registration Number: 80132390013
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FAMÍLIA DIMER ONE PLUS
Risk Class III

Registration Details

80132390013

25351656673202101

61058400000142

Company Information

Brazil
PT: BRASIL

Dates and Status

Aug 09, 2021

09/08/2031

09/18/2025 19:00:01