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Single-use cardiac electrophysiology catheter - ANVISA Registration 80224390183

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 80224390183 and manufactured by VASCOMED GMBH. The registration is held by BIOTRONIK COMERCIAL MÉDICA LTDA. with validity until Feb 28, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80224390183
2 Related Devices
Registration Details
ANVISA Registration Number: 80224390183
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Related Devices (2)

CATETER DEFLECTÍVEL DE ABLAÇÃO E MAPEAMENTO - ALCATH GOLD FULLCIRCLE
Risk Class IV

Registration Details

80224390183

25351102378201068

50595271000105

Company Information

VASCOMED GMBH
Germany
PT: ALEMANHA

Dates and Status

Feb 28, 2011

28/02/2026

09/18/2025 19:00:01

CATETER DEFLECTÍVEL DE ABLAÇÃO E MAPEAMENTO - ALCATH GOLD FULLCIRCLE
Risk Class IV

Registration Details

80224390183

25351102378201068

50595271000105

Company Information

Dates and Status

Feb 28, 2011

28/02/2026

09/18/2025 19:00:01