CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 10349000468

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 10349000468 and manufactured by EV3. INC. The registration is held by AUTO SUTURE DO BRASIL LTDA. with validity until Nov 11, 2028.

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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
10349000468
2 Related Devices
Registration Details
ANVISA Registration Number: 10349000468
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (2)

Registration Details

10349000468

25351481864201412

01645409000128

Company Information

EV3. INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 22, 2015

11/11/2028

09/18/2025 19:00:01

Registration Details

10349000468

25351481864201412

01645409000128

Company Information

Dates and Status

Jun 22, 2015

11/11/2028

09/18/2025 19:00:01