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ANVISA registration 10275160052Valid until Apr 17, 2027

Neurology Diagnostic Equipment

ANVISA Registration Number: 10275160052SUPORTE HOSPITALAR LTDAHEMEDEX INCRisk Class IV
Verified
Device names
Technical name
Neurology Diagnostic Equipment
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PT: Equipamento de Diagnóstico em Neurologia
Commercial name
QFlow 500 Titanium Bolt - Quad Lumen Bolt Kit
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Risk class
Class IV
Registration details
Registration Number
10275160052
Process Number
25351829143201697
CNPJ
73857393000128
Company information
Registration Holder
SUPORTE HOSPITALAR LTDA
Manufacturer
HEMEDEX INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Apr 17, 2017
Validity
17/04/2027
Last Updated
08/18/2026 19:00:00
About this record

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 shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.