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INTRAVASCULAR FILTER AND ASSOCIATED DEVICES - ANVISA Registration 80633660018

Access comprehensive regulatory information for INTRAVASCULAR FILTER AND ASSOCIATED DEVICES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80633660018 and manufactured by manufacturer not specified. The registration is held by IGI COMERCIO DE EQUIPAMENTOS ELETRONICOS LTDA with validity until Nov 25, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including CORDIS CORPORATION, ALN IMPLANTS CHIRURGICAUX, 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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80633660018
2 Related Devices
Registration Details
ANVISA Registration Number: 80633660018
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Related Devices (2)

Filtro de Veia Cava Opcional com Gancho ALN โ€“ FPH.OATF
Risk Class IV

Registration Details

80633660018

25351652020202225

10394359000144

Company Information

Dates and Status

Nov 25, 2024

25/11/2034

09/18/2025 19:00:01

Filtro de Veia Cava Opcional com Gancho ALN โ€“ FPH.OATF
Risk Class IV

Registration Details

80633660018

25351652020202225

10394359000144

Company Information

France
PT: FRANร‡A

Dates and Status

Nov 25, 2024

25/11/2034

09/18/2025 19:00:01