Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

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, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
2 Competitors
3 Recent Registrations
10275160052
2 Related Devices
Registration Details
ANVISA Registration Number: 10275160052
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

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

Companies Making Similar Products
Top companies providing products with the same technical name: "Neurology Diagnostic Equipment"