Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Device for Maxillary Fixation - ANVISA Registration 82673019011

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 II medical device is registered under ANVISA number 82673019011 and manufactured by GENIUS DESENVOLVIMENTO E INDUSTRIA DE DISPOSITIVOS MEDICOS LTDA. The registration is held by GENIUS DESENVOLVIMENTO E INDUSTRIA DE DISPOSITIVOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
82673019011
Registration Details
ANVISA Registration Number: 82673019011
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Parafuso de Bloqueio Intermaxilar Genius
Risk Class II

Registration Details

82673019011

25351059131202519

47344749000110

Company Information

Dates and Status

May 05, 2025

VIGENTE

09/18/2025 19:00:01