Neurology Diagnostic Equipment - ANVISA Registration 10166369001

Access comprehensive regulatory information for Neurology Diagnostic Equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10166369001 and manufactured by HP BIOPROTESES LTDA. The registration is held by HP BIOPROTESES 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, 1 companies making the same product including HEMEDEX INC, and 4 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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10166369001
Registration Details
ANVISA Registration Number: 10166369001
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

DISPOSITIVO DE REGULAGEM PARA VÁLVULA PROGRAMÁVEL SPHERA PRO
Risk Class I

Registration Details

10166369001

25351710777201418

54801196000142

Company Information

Brazil
PT: BRASIL

Dates and Status

Dec 08, 2014

VIGENTE

09/18/2025 19:00:01

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