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DRUG-ELUTING STENT FOR CORONARY ARTERIES - ANVISA Registration 80224390311

Access comprehensive regulatory information for DRUG-ELUTING STENT FOR CORONARY ARTERIES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80224390311 and manufactured by BIOTRONIK AG. The registration is held by BIOTRONIK COMERCIAL MÉDICA LTDA. with validity until Dec 26, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80224390311
2 Related Devices
Registration Details
ANVISA Registration Number: 80224390311
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Related Devices (2)

SYNSIRO PRO - SISTEMA DE STENT CORONÁRIO COM ELUIÇÃO DE SIROLIMUS
Risk Class IV

Registration Details

80224390311

25351659074202211

50595271000105

Company Information

BIOTRONIK AG
Switzerland
PT: SUÍÇA

Dates and Status

Dec 26, 2023

26/12/2033

09/18/2025 19:00:01

SYNSIRO PRO - SISTEMA DE STENT CORONÁRIO COM ELUIÇÃO DE SIROLIMUS
Risk Class IV

Registration Details

80224390311

25351659074202211

50595271000105

Company Information

Dates and Status

Dec 26, 2023

26/12/2033

09/18/2025 19:00:01