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Tracheal Tube - ANVISA Registration 10297020093

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 10297020093 and manufactured by ELECTROPLAST S.A. 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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10297020093
Registration Details
ANVISA Registration Number: 10297020093
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Device Details

SONDA / TUBO ENDOTRAQUEAL COM BALÃO E VIA DE ASPIRAÇÃO SUBGLÓTICA, BCI MEDICAL
Risk Class II

Registration Details

10297020093

25351420097201367

43566371000148

Company Information

ELECTROPLAST S.A
Uruguay
PT: URUGUAI

Dates and Status

Oct 21, 2013

VIGENTE

09/18/2025 19:00:01