Neurology Diagnostic Equipment - ANVISA Registration 10275160045
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 10275160045 and manufactured by manufacturer not specified. The registration is held by SUPORTE HOSPITALAR LTDA with validity until May 09, 2026.
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.
Related Devices (2)
Registration Details
10275160045
25351831026201618
73857393000128
Company Information
Dates and Status
May 09, 2016
09/05/2026
09/18/2025 19:00:01
Equipamento de Diagnóstico em Neurologia
QFlow 500 Titanium Bolt - Quad Lumen Bolt Kit
HEMEDEX INC
10275160052
Apr 17, 2017
Equipamento de Diagnóstico em Neurologia
QFlow 500 Titanium Bolt - Quad Lumen Bolt Kit
Not specified
10275160052
Apr 17, 2017
Equipamento de Diagnóstico em Neurologia
DISPOSITIVO DE REGULAGEM PARA VÁLVULA PROGRAMÁVEL SPHERA PRO
HP BIOPROTESES LTDA
10166369001
Dec 08, 2014

