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Device for Maxillary Fixation - ANVISA Registration 80271810128

Access comprehensive regulatory information for Device for Maxillary Fixation in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80271810128 and manufactured by MEDARTIS AG. The registration is held by MEDARTIS IMPORTACAO E EXPORTACAO LTDA with validity until Feb 17, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA., TECHIMPORT TECNOLOGIA EM IMPLANTES ORTOPEDICOS LTDA, 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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80271810128
2 Related Devices
Registration Details
ANVISA Registration Number: 80271810128
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Related Devices (2)

MODUS® 2 Sistema de Fixação Intermaxilar IMF
Risk Class III

Registration Details

80271810128

25351242937202487

07021336000180

Company Information

MEDARTIS AG
Switzerland
PT: SUÍÇA

Dates and Status

Feb 17, 2025

17/02/2035

09/18/2025 19:00:01

MODUS® 2 Sistema de Fixação Intermaxilar IMF
Risk Class III

Registration Details

80271810128

25351242937202487

07021336000180

Company Information

Dates and Status

Feb 17, 2025

17/02/2035

09/18/2025 19:00:01