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Tracheal Tube - ANVISA Registration 10297020101

Access comprehensive regulatory information for Tracheal 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 10297020101 and manufactured by HAIYAN KANGYUAN MEDICAL INSTRUMENT CO., LTD. The registration is held by BADEIA COMERCIO IMPORTAÇÃO 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 ZHANJIANG STAR ENTERPRISE CO,.LTD, HANGZHOU FORMED MEDICAL DEVICES 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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10297020101
Registration Details
ANVISA Registration Number: 10297020101
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Device Details

Comercial Sonda/Tubo Endotraqueal Aramada sem Balão Estéril Madewell
Risk Class II

Registration Details

10297020101

25351312395201950

43566371000148

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jul 01, 2019

VIGENTE

09/18/2025 19:00:01