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.
Related Devices (2)
Registration Details
10275160052
25351829143201697
73857393000128
Company Information
Dates and Status
Apr 17, 2017
17/04/2027
09/18/2025 19:00:01
Equipamento de Diagnóstico em Neurologia
QFLOW 500 PERFUSION PROBE
Not specified
10275160045
May 09, 2016
Equipamento de Diagnóstico em Neurologia
QFLOW 500 PERFUSION PROBE
HEMEDEX INC
10275160045
May 09, 2016
Equipamento de Diagnóstico em Neurologia
DISPOSITIVO DE REGULAGEM PARA VÁLVULA PROGRAMÁVEL SPHERA PRO
HP BIOPROTESES LTDA
10166369001
Dec 08, 2014

