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ANVISA registration 80898209027Active

Guide Wire

ANVISA Registration Number: 80898209027LAIBO MEDICAL PRODUTOS MEDICOS E HOSPITALARES LTDANEWTECH MEDICAL DEVICESRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
ClearGWire™ - Guide Wire
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Risk class
Class II
Registration details
Registration Number
80898209027
Process Number
25351094284202685
CNPJ
14477127000100
Company information
Registration Holder
LAIBO MEDICAL PRODUTOS MEDICOS E HOSPITALARES LTDA
Manufacturer
NEWTECH MEDICAL DEVICES
Manufacturing Country
India
PT: ÍNDIA
Dates and status
Publication Date
Jul 20, 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 80898209027 and manufactured by NEWTECH MEDICAL DEVICES. The registration is held by LAIBO MEDICAL PRODUTOS MEDICOS E HOSPITALARES 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.