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CORONARY ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 80788620023

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 80788620023 and manufactured by Rontis Corporation S.A.. The registration is held by NIPRO MEDICAL CORPORATION PRODUTOS MÉDICOS LTDA with validity until Mar 28, 2026.

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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80788620023
2 Related Devices
Registration Details
ANVISA Registration Number: 80788620023
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Related Devices (2)

Cateter Balão Coronário de Oclusão Total Crônica Europa Ultra CTO OTW
Risk Class IV

Registration Details

80788620023

25351558250201509

13333090000184

Company Information

Switzerland
PT: SUÍÇA

Dates and Status

Mar 28, 2016

28/03/2026

09/18/2025 19:00:01

Cateter Balão Coronário de Oclusão Total Crônica Europa Ultra CTO OTW
Risk Class IV

Registration Details

80788620023

25351558250201509

13333090000184

Company Information

Dates and Status

Mar 28, 2016

28/03/2026

09/18/2025 19:00:01