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External Fixators - ANVISA Registration 82117660026

Access comprehensive regulatory information for External Fixators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82117660026 and manufactured by AIKE (SHANGHAI) MEDICAL INSTRUMENT CO., LTD. The registration is held by BFIX INTERNACIONAL COMERCIAL IMPORTADORA DE PRODUTOS 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 G D RUFINO LTDA EPP, CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos 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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82117660026
Registration Details
ANVISA Registration Number: 82117660026
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Device Details

SISTEMA DE COTOVELO FLUTUANTE BFIX
Risk Class I

Registration Details

82117660026

25351457872202472

12437644000120

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 13, 2025

VIGENTE

09/18/2025 19:00:01