QFlow 500 Titanium Bolt - Single Lumen Bolt Kit

Diagnostic device · class IV · Until 24/10/2026

Registration no.
10275160049
Process no.
25351830913201609
Status
Until 24/10/2026
Device type
Diagnostic device (DISPOSITIVO PARA DIAGNÓSTICO)
Risk class
IV
Registration holder
SUPORTE HOSPITALAR LTDA CNPJ 73.857.393/0001-28 · 82 registrations
Manufacturer
HEMEDEX INC · United States
Published
24/10/2016
Valid until
24/10/2026
Last updated by ANVISA
2026-10-12
Official record
View on ANVISA ↗

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