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CORONARY ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 81667100007

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 81667100007 and manufactured by manufacturer not specified. The registration is held by MICROPORT SCIENTIFIC VASCULAR BRASIL LTDA with validity until Dec 28, 2025.

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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81667100007
2 Related Devices
Registration Details
ANVISA Registration Number: 81667100007
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Related Devices (2)

Foxtrot PRO Cateter Balão para PTCA
Risk Class IV
Expired

Registration Details

81667100007

25351694936201876

29182018000133

Company Information

Dates and Status

Oct 22, 2018

28/12/2025

09/18/2025 19:00:01

Foxtrot PRO Cateter Balão para PTCA
Risk Class IV
Expired

Registration Details

81667100007

25351694936201876

29182018000133

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 22, 2018

28/12/2025

09/18/2025 19:00:01