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ANVISA registration 80386689020Active

EEG Monitor

ANVISA Registration Number: 80386689020med 7 produtos hospitalares ltda eppCADWELL INDUSTRIES, INC.Risk Class II
Verified
Device names
Technical name
EEG Monitor
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PT: Monitor de EEG
Commercial name
Cascade Iomax
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Risk class
Class II
Registration details
Registration Number
80386689020
Process Number
25351043476202623
CNPJ
08140941000132
Company information
Registration Holder
med 7 produtos hospitalares ltda epp
Manufacturer
CADWELL INDUSTRIES, INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Apr 13, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for EEG Monitor in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80386689020 and manufactured by CADWELL INDUSTRIES, INC.. The registration is held by med 7 produtos hospitalares ltda epp 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.