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DRUG-ELUTING STENT FOR CORONARY ARTERIES - ANVISA Registration 80102511720

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 80102511720 and manufactured by BIOSENSORS EUROPE SA. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Nov 21, 2026.

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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80102511720
2 Related Devices
Registration Details
ANVISA Registration Number: 80102511720
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Related Devices (2)

STENT CORONÁRIO BIOFREEDOM COM REVESTIMENTO DE FÁRMACO
Risk Class IV

Registration Details

80102511720

25351978292201603

04718143000194

Company Information

Switzerland
PT: SUÍÇA

Dates and Status

Nov 21, 2016

21/11/2026

09/18/2025 19:00:01

STENT CORONÁRIO BIOFREEDOM COM REVESTIMENTO DE FÁRMACO
Risk Class IV

Registration Details

80102511720

25351978292201603

04718143000194

Dates and Status

Nov 21, 2016

21/11/2026

09/18/2025 19:00:01