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INTRAVASCULAR MICROPERFUSION CATHETER - ANVISA Registration 81576620022

Access comprehensive regulatory information for INTRAVASCULAR MICROPERFUSION CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81576620022 and manufactured by CORDIS US CORP.. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until Feb 07, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including VASCULAR SOLUTIONS, LLC, STRYKER NEUROVASCULAR, 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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81576620022
2 Related Devices
Registration Details
ANVISA Registration Number: 81576620022
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Related Devices (2)

CATETER DE DIAGNÓSTICO CORDIS INFINITI™
Risk Class IV

Registration Details

81576620022

25351103379202354

27548227000122

Company Information

CORDIS US CORP.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 06, 2023

07/02/2026

09/18/2025 19:00:01

CATETER DE DIAGNÓSTICO CORDIS INFINITI™
Risk Class IV

Registration Details

81576620022

25351103379202354

27548227000122

Company Information

Dates and Status

Mar 06, 2023

07/02/2026

09/18/2025 19:00:01