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ANVISA registration 80073110097Active

Guide Wire

ANVISA Registration Number: 80073110097MEDI-GLOBE BRASIL LTDAUROVISION GMBHRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO GUIA PARA USO UROLÓGICO
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Risk class
Class II
Registration details
Registration Number
80073110097
Process Number
25351038759201843
CNPJ
04242860000192
Company information
Registration Holder
MEDI-GLOBE BRASIL LTDA
Manufacturer
UROVISION GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Feb 19, 2018
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 80073110097 and manufactured by UROVISION GMBH. The registration is held by MEDI-GLOBE BRASIL 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.