Blood Filter/Arterial Filter - ANVISA Registration 10154459032

Access comprehensive regulatory information for Blood Filter/Arterial Filter in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10154459032 and manufactured by FRESENIUS KABI AG. The registration is held by FRESENIUS HEMOCARE BRASIL LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MEDTRONIC, INC., CARDIO MEDICAL INDUSTRIAL LTDA, and 5 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.

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10154459032
Registration Details
ANVISA Registration Number: 10154459032
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Filtro para Hemocomponentes com penetrador ventilado e conector luer
Risk Class II

Registration Details

10154459032

25351030628202113

49601107000184

Company Information

FRESENIUS KABI AG
Germany
PT: ALEMANHA

Dates and Status

Dec 16, 2021

VIGENTE

09/18/2025 19:00:01