CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 10216710398

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10216710398 and manufactured by VOLCANO CORPORATION. The registration is held by PHILIPS MEDICAL SYSTEMS LTDA with validity until Aug 23, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ABBOTT MEDICAL, COOK INCORPORATED, 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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10216710398
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Registration Details
ANVISA Registration Number: 10216710398
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Related Devices (2)

Fio-Guia de Pressão OmniWire
Risk Class IV

Registration Details

10216710398

25351881282202114

58295213000178

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 23, 2021

23/08/2031

09/18/2025 19:00:01

Fio-Guia de Pressão OmniWire
Risk Class IV

Registration Details

10216710398

25351881282202114

58295213000178

Company Information

Dates and Status

Aug 23, 2021

23/08/2031

09/18/2025 19:00:01