MYOGLOBIN - CLASS II - ANVISA Registration 80102512660

Access comprehensive regulatory information for MYOGLOBIN - CLASS II in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102512660 and manufactured by RESPONSE BIOMEDICAL CORP.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

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, SIEMENS HEALTHCARE DIAGNOSTICS 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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80102512660
Registration Details
ANVISA Registration Number: 80102512660
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

RAMP® Mioglobina
Risk Class II

Registration Details

80102512660

25351491317202127

04718143000194

Company Information

Canada
PT: CANADÁ

Dates and Status

May 20, 2021

VIGENTE

09/18/2025 19:00:01