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CORONARY ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 10407990087

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 10407990087 and manufactured by manufacturer not specified. The registration is held by ANGIOMED IMPORTACAO E EXPORTACAO LTDA with validity until May 11, 2030.

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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10407990087
2 Related Devices
Registration Details
ANVISA Registration Number: 10407990087
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Related Devices (2)

Simpass CTO RX Cateter Balão para PTCA
Risk Class IV

Registration Details

10407990087

25351584206201949

02699256000164

Company Information

Dates and Status

May 11, 2020

11/05/2030

09/18/2025 19:00:01

Simpass CTO RX Cateter Balão para PTCA
Risk Class IV

Registration Details

10407990087

25351584206201949

02699256000164

Company Information

Turkey
PT: TURQUIA

Dates and Status

May 11, 2020

11/05/2030

09/18/2025 19:00:01