septal occluder - ANVISA Registration 80202910071

Access comprehensive regulatory information for septal occluder in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80202910071 and manufactured by manufacturer not specified. The registration is held by TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA with validity until Apr 22, 2034.

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 VASCULAR INNOVATIONS CO. LTD, SHANGHAI SHAPE MEMORY ALLOY 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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80202910071
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Registration Details
ANVISA Registration Number: 80202910071
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

FIGULLA FLEX II UNI
Risk Class IV

Registration Details

80202910071

25351188515201313

05638301000169

Company Information

Dates and Status

Apr 22, 2014

22/04/2034

09/18/2025 19:00:01

FIGULLA FLEX II UNI
Risk Class IV

Registration Details

80202910071

25351188515201313

05638301000169

Company Information

OCCLUTECH GMBH
Germany
PT: ALEMANHA

Dates and Status

Apr 22, 2014

22/04/2034

09/18/2025 19:00:01