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ANVISA registration 80073110094Active

Guide Wire

ANVISA Registration Number: 80073110094MEDI-GLOBE BRASIL LTDAUROVISION GMBHRisk Class I
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO GUIA TEFLONADO
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Risk class
Class I
Registration details
Registration Number
80073110094
Process Number
25351038737201883
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 I medical device is registered under ANVISA number 80073110094 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.