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External Fixators - ANVISA Registration 80203020057

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 80203020057 and manufactured by CITIEFFE S.R.L.. The registration is held by BONE SURGICAL EQUIPAMENTOS 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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80203020057
Registration Details
ANVISA Registration Number: 80203020057
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Device Details

Fixador Externo Rekrea
Risk Class I

Registration Details

80203020057

25351885504201628

04408009000197

Company Information

CITIEFFE S.R.L.
Italy
PT: ITÁLIA

Dates and Status

Jul 11, 2016

VIGENTE

09/18/2025 19:00:01