Single-use cardiac electrophysiology catheter - ANVISA Registration 81667100052

Access comprehensive regulatory information for Single-use cardiac electrophysiology 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 81667100052 and manufactured by SHANGHAI MICROPORT EP MEDTECH CO., LTD. The registration is held by MICROPORT SCIENTIFIC VASCULAR BRASIL LTDA with validity until Jul 11, 2032.

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 ABBOTT MEDICAL, SHANGHAI MICROPORT EP MEDTECH 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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81667100052
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Registration Details
ANVISA Registration Number: 81667100052
Janaina dos Santos de Miranda

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Related Devices (2)

Cateter de Diagnóstico com Curva Dirigível Easyfinder 3D
Risk Class IV

Registration Details

81667100052

25351126201202209

29182018000133

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jul 11, 2022

11/07/2032

09/18/2025 19:00:01

Cateter de Diagnóstico com Curva Dirigível Easyfinder 3D
Risk Class IV

Registration Details

81667100052

25351126201202209

29182018000133

Company Information

Dates and Status

Jul 11, 2022

11/07/2032

09/18/2025 19:00:01