D-DIMER - ANVISA Registration 80102513226

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 80102513226 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 08, 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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80102513226
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Registration Details
ANVISA Registration Number: 80102513226
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Controles D-Dímero RAMP
Risk Class III

Registration Details

80102513226

25351638621202314

04718143000194

Dates and Status

Apr 08, 2024

08/04/2034

09/18/2025 19:00:01

Família Controles D-Dímero RAMP
Risk Class III

Registration Details

80102513226

25351638621202314

04718143000194

Company Information

Canada
PT: CANADÁ

Dates and Status

Apr 08, 2024

08/04/2034

09/18/2025 19:00:01