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embolic protection device - ANVISA Registration 10349000462

Access comprehensive regulatory information for embolic protection device in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10349000462 and manufactured by EV3, INC.. The registration is held by AUTO SUTURE DO BRASIL LTDA. with validity until Apr 29, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including LEMAITRE VASCULAR INC, BEIJING TAIJIEWEIYE TECHNOLOGY CO., LTD, 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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10349000462
2 Related Devices
Registration Details
ANVISA Registration Number: 10349000462
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Related Devices (2)

Dispositivo de Proteção Embólica SpiderFX
Risk Class IV

Registration Details

10349000462

25351481370201479

01645409000128

Company Information

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

Dates and Status

Jun 22, 2015

29/04/2028

09/18/2025 19:00:01

Dispositivo de Proteção Embólica SpiderFX
Risk Class IV

Registration Details

10349000462

25351481370201479

01645409000128

Company Information

Dates and Status

Jun 22, 2015

29/04/2028

09/18/2025 19:00:01

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