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Endobronchial Tube - ANVISA Registration 80480059004

Access comprehensive regulatory information for Endobronchial Tube in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80480059004 and manufactured by SHREE UMIYA SURGICAL PVT. LTD.. The registration is held by ATUAL COMERCIO E REPRESENTACOES 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 Hangzhou tappa medical Technology Co. Ltd., SHENZHEN INSIGHTERS MEDICAL TECHNOLOGY CO., LTD, 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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80480059004
Registration Details
ANVISA Registration Number: 80480059004
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Device Details

TUBO ENDOTRAQUEAL MEDIPLUS
Risk Class II

Registration Details

80480059004

25351049968202541

08955615000183

Company Information

India
PT: รNDIA

Dates and Status

Apr 28, 2025

VIGENTE

09/18/2025 19:00:01