Pure Global

septal occluder - ANVISA Registration 80102512486

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 80102512486 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS Mร‰DICOS LTDA with validity until May 25, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including VASCULAR INNOVATIONS CO. LTD, LIFETECH SCIENTIFIC (SHENZHEN) 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80102512486
2 Related Devices
Registration Details
ANVISA Registration Number: 80102512486
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Related Devices (2)

Oclusor MemoPart PDA
Risk Class IV

Registration Details

80102512486

25351827702201808

04718143000194

Dates and Status

May 25, 2020

25/05/2030

09/18/2025 19:00:01

Oclusor MemoPart PDA
Risk Class IV

Registration Details

80102512486

25351827702201808

04718143000194

Company Information

China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

May 25, 2020

25/05/2030

09/18/2025 19:00:01