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ANVISA registration 80835379010Active

Electromyographic endotracheal tube electrode

ANVISA Registration Number: 80835379010MIT MEDICAL INDUSTRY TECHNOLOGY LTDA - MEMIT MEDICAL INDUSTRY TECHNOLOGY LTDA - MERisk Class II
Verified
Device names
Technical name
Electromyographic endotracheal tube electrode
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PT: Eletrodo de tubo endotraqueal eletromiográfico
Commercial name
KIT CÂNULA MONITORIZACAO FACIAL
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Risk class
Class II
Registration details
Registration Number
80835379010
Process Number
25351040308202503
CNPJ
10795989000120
Company information
Registration Holder
MIT MEDICAL INDUSTRY TECHNOLOGY LTDA - ME
Manufacturer
MIT MEDICAL INDUSTRY TECHNOLOGY LTDA - ME
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Apr 22, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Electromyographic endotracheal tube electrode in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80835379010 and manufactured by MIT MEDICAL INDUSTRY TECHNOLOGY LTDA - ME. The registration is held by MIT MEDICAL INDUSTRY TECHNOLOGY LTDA - ME with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.