Neurology Diagnostic Equipment - ANVISA Registration 10275160052

Access comprehensive regulatory information for Neurology Diagnostic Equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10275160052 and manufactured by HEMEDEX INC. The registration is held by SUPORTE HOSPITALAR LTDA with validity until Apr 17, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including HP BIOPROTESES LTDA, HEMEDEX INC, and 3 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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10275160052
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Registration Details
ANVISA Registration Number: 10275160052
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

QFlow 500 Titanium Bolt - Quad Lumen Bolt Kit
Risk Class IV

Registration Details

10275160052

25351829143201697

73857393000128

Company Information

HEMEDEX INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 17, 2017

17/04/2027

09/18/2025 19:00:01

QFlow 500 Titanium Bolt - Quad Lumen Bolt Kit
Risk Class IV

Registration Details

10275160052

25351829143201697

73857393000128

Company Information

Dates and Status

Apr 17, 2017

17/04/2027

09/18/2025 19:00:01

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