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ANVISA registration 81637619075Active

Guide Wire

ANVISA Registration Number: 81637619075Humanna Medical LtdaHumanna Medical LtdaRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Introdutor de Cateter de ICG Tumoral Delimitation System (Tumoral, perfusão sanguínea)
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Risk class
Class II
Registration details
Registration Number
81637619075
Process Number
25351090587202629
CNPJ
27617206000111
Company information
Registration Holder
Humanna Medical Ltda
Manufacturer
Humanna Medical Ltda
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Jun 01, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81637619075 and manufactured by Humanna Medical Ltda. The registration is held by Humanna Medical Ltda 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.