PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 80202910112

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 80202910112 and manufactured by manufacturer not specified. The registration is held by TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA with validity until Jul 07, 2035.

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 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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80202910112
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Registration Details
ANVISA Registration Number: 80202910112
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Registration Details

80202910112

25351391217202363

05638301000169

Company Information

Dates and Status

Jul 07, 2025

07/07/2035

09/18/2025 19:00:01

Registration Details

80202910112

25351391217202363

05638301000169

Company Information

Lithuania
PT: LITUÂNIA

Dates and Status

Jul 07, 2025

07/07/2035

09/18/2025 19:00:01