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Tracheal Tube - ANVISA Registration 80342239022

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 80342239022 and manufactured by PLASTIFLEX NORTH CAROLINA, LLC. The registration is held by NEUROSOFT EQUIPAMENTOS E SUPRIMENTOS 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 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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80342239022
Registration Details
ANVISA Registration Number: 80342239022
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Device Details

TUBO TRAQUEAL
Risk Class II

Registration Details

80342239022

25351036746201703

08172474000122

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Mar 06, 2017

VIGENTE

09/18/2025 19:00:01