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Bone Distractor - ANVISA Registration 81666779001

Access comprehensive regulatory information for Bone Distractor in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81666779001 and manufactured by AREX. The registration is held by VISAO IMPORTADORA E DISTRIBUIDORA DE MATERIAIS MEDICOS UNIPESSOAL 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 ENGIMPLAN ENGENHARIA DE IMPLANTE IND E COM LTDA, TRAUMEC TECNOLOGIA E IMPLANTES ORTOPÉDICOS IMP. E EXP. LTDA - EPP, 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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81666779001
Registration Details
ANVISA Registration Number: 81666779001
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Device Details

Distrator Dinâmico para Articulação de Dedo - LTX
Risk Class II

Registration Details

81666779001

25351131562202188

30049016000150

Company Information

AREX
France
PT: FRANÇA

Dates and Status

Mar 11, 2021

VIGENTE

09/18/2025 19:00:01