septal occluder - ANVISA Registration 80102512672

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 80102512672 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jun 21, 2031.

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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80102512672
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Registration Details
ANVISA Registration Number: 80102512672
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Oclusor CeraFlex™ PFO
Risk Class IV

Registration Details

80102512672

25351899707202061

04718143000194

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 21, 2021

21/06/2031

09/18/2025 19:00:01

Oclusor CeraFlex™ PFO
Risk Class IV

Registration Details

80102512672

25351899707202061

04718143000194

Dates and Status

Jun 21, 2021

21/06/2031

09/18/2025 19:00:01