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Implantable Device Programmer - ANVISA Registration 80224390299

Access comprehensive regulatory information for Implantable Device Programmer in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80224390299 and manufactured by BIOTRONIK SE & CO KG. The registration is held by BIOTRONIK COMERCIAL MÉDICA LTDA. with validity until Jul 19, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including MEDTRONIC, INC., ABBOTT MEDICAL, 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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80224390299
2 Related Devices
Registration Details
ANVISA Registration Number: 80224390299
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Related Devices (2)

RENAMIC NEO - SISTEMA DE PROGRAMAÇÃO E MONITORAÇÃO PARA MARCAPASSOS CARDÍACOS E CARDIOVERSORES DESFI
Risk Class III

Registration Details

80224390299

25351722299202131

50595271000105

Company Information

Germany
PT: ALEMANHA

Dates and Status

Jul 19, 2021

19/07/2031

09/18/2025 19:00:01

RENAMIC NEO - SISTEMA DE PROGRAMAÇÃO E MONITORAÇÃO PARA MARCAPASSOS CARDÍACOS E CARDIOVERSORES DESFI
Risk Class III

Registration Details

80224390299

25351722299202131

50595271000105

Company Information

Dates and Status

Jul 19, 2021

19/07/2031

09/18/2025 19:00:01