PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 81576620023

Access comprehensive regulatory information for PERIPHERAL 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 81576620023 and manufactured by CORDIS CASHEL. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until Nov 12, 2027.

This page provides complete technical specifications for 3 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION, BROSMED MEDICAL CO., LTD, 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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81576620023
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Registration Details
ANVISA Registration Number: 81576620023
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (3)

Registration Details

81576620023

25351103400202311

27548227000122

Company Information

CORDIS CASHEL
Ireland
PT: IRLANDA

Dates and Status

Mar 06, 2023

12/11/2027

09/18/2025 19:00:01

Registration Details

81576620023

25351103400202311

27548227000122

Company Information

Dates and Status

Mar 06, 2023

12/11/2027

09/18/2025 19:00:01

Registration Details

81576620023

25351103400202311

27548227000122

Company Information

CORDIS EUROPA N.V.
Netherlands
PT: HOLANDA (PAÍSES BAIXOS)

Dates and Status

Mar 06, 2023

12/11/2027

09/18/2025 19:00:01