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Catheter Fixation Device - ANVISA Registration 80022069036

Access comprehensive regulatory information for Catheter Fixation Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80022069036 and manufactured by FUJIFILM MEDWORK GMBH. The registration is held by FUJIFILM DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including PHARMAPLAST S.A.E, BARD ACCESS SYSTEMS, INC., 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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80022069036
Registration Details
ANVISA Registration Number: 80022069036
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Device Details

Fixador do fio guia โ€“ SPE1-Y
Risk Class II

Registration Details

80022069036

25351323288202414

60397874000156

Company Information

Germany
PT: ALEMANHA

Dates and Status

Jun 17, 2024

VIGENTE

09/18/2025 19:00:01