ENDOCARDIAL DEFIBRILLATION CABLE/ELECTRODE - ANVISA Registration 80224390267

Access comprehensive regulatory information for ENDOCARDIAL DEFIBRILLATION CABLE/ELECTRODE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80224390267 and manufactured by BIOTRONIK SE & CO KG. The registration is held by BIOTRONIK COMERCIAL MÉDICA LTDA. with validity until Jan 30, 2027.

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, MEDTRONIC, INC., 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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80224390267
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Registration Details
ANVISA Registration Number: 80224390267
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

PLEXA DF-1 - ELETRODO DE FIXAÇÁO ATIVA PARA CARDIOVERSOR DESFIBRILADOR IMPLANTÁVEL condicional para Ressonância Magnética (ProMRI).
Risk Class IV

Registration Details

80224390267

25351537615201601

50595271000105

Company Information

Germany
PT: ALEMANHA

Dates and Status

Jan 30, 2017

30/01/2027

09/18/2025 19:00:01

PLEXA DF-1 - ELETRODO DE FIXAÇÁO ATIVA PARA CARDIOVERSOR DESFIBRILADOR IMPLANTÁVEL condicional para Ressonância Magnética (ProMRI).
Risk Class IV

Registration Details

80224390267

25351537615201601

50595271000105

Company Information

Dates and Status

Jan 30, 2017

30/01/2027

09/18/2025 19:00:01