TROPONIN - ANVISA Registration 80102512686

Access comprehensive regulatory information for TROPONIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102512686 and manufactured by RESPONSE BIOMEDICAL CORP.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Aug 09, 2031.

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, BODITECH MED INC., 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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80102512686
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Registration Details
ANVISA Registration Number: 80102512686
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

RAMP® Troponina I
Risk Class III

Registration Details

80102512686

25351491162202129

04718143000194

Company Information

Canada
PT: CANADÁ

Dates and Status

Aug 09, 2021

09/08/2031

09/18/2025 19:00:01

RAMP® Troponina I
Risk Class III

Registration Details

80102512686

25351491162202129

04718143000194

Dates and Status

Aug 09, 2021

09/08/2031

09/18/2025 19:00:01