CORONARY ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 80120820037

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 80120820037 and manufactured by BALTON SP. Z.O.O.. The registration is held by BIOLINE COMERCIAL LTDA with validity until Apr 19, 2031.

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 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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80120820037
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Registration Details
ANVISA Registration Number: 80120820037
Janaina dos Santos de Miranda

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Related Devices (2)

CATETER DE ANGIOPLASTIA CORONARIANA RIVER CTO
Risk Class IV

Registration Details

80120820037

25351796912202075

04762934000111

Company Information

BALTON SP. Z.O.O.
Poland
PT: POLÔNIA

Dates and Status

Apr 19, 2021

19/04/2031

09/18/2025 19:00:01

CATETER DE ANGIOPLASTIA CORONARIANA RIVER CTO
Risk Class IV

Registration Details

80120820037

25351796912202075

04762934000111

Company Information

Dates and Status

Apr 19, 2021

19/04/2031

09/18/2025 19:00:01