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CORONARY ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 10407990091

Access comprehensive regulatory information for CORONARY ANGIOPLASTY BALLOON 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 10407990091 and manufactured by manufacturer not specified. The registration is held by ANGIOMED IMPORTACAO E EXPORTACAO LTDA with validity until Apr 01, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD, BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, 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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10407990091
2 Related Devices
Registration Details
ANVISA Registration Number: 10407990091
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Related Devices (2)

Simvalve Flex - Cateter Balão para Valvuloplastia
Risk Class IV

Registration Details

10407990091

25351120312202384

02699256000164

Company Information

Dates and Status

Apr 01, 2024

01/04/2034

09/18/2025 19:00:01

Simvalve Flex - Cateter Balão para Valvuloplastia
Risk Class IV

Registration Details

10407990091

25351120312202384

02699256000164

Company Information

Turkey
PT: TURQUIA

Dates and Status

Apr 01, 2024

01/04/2034

09/18/2025 19:00:01