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Silicone Gel Sheet - ANVISA Registration 83206730001

Access comprehensive regulatory information for Silicone Gel Sheet in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 83206730001 and manufactured by INStituto de bioengenharia erasto gaertner ltda. The registration is held by INStituto de bioengenharia erasto gaertner 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 BIODERMIS CORPORATION, CLAUDIONEIA DADAS DE OLIVEIRA FABRICACAO MATERIAIS PARA MEDICINA, 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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83206730001
Registration Details
ANVISA Registration Number: 83206730001
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Device Details

Fita Gel de Silicone IBEG
Risk Class I

Registration Details

83206730001

25351123729202561

56961698000166

Company Information

Brazil
PT: BRASIL

Dates and Status

Aug 04, 2025

VIGENTE

09/18/2025 19:00:01