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ANVISA registration 10334780044Active

Guide Wire

ANVISA Registration Number: 10334780044G.F.E. DO BRASIL LTDA.ENDO-FLEX GMBHRisk Class I
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Nitinol
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Risk class
Class I
Registration details
Registration Number
10334780044
Process Number
25351382264201189
CNPJ
55126981000100
Company information
Registration Holder
G.F.E. DO BRASIL LTDA.
Manufacturer
ENDO-FLEX GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Aug 15, 2011
Status
Active
Official value: VIGENTE
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 10334780044 and manufactured by ENDO-FLEX GMBH. The registration is held by G.F.E. DO 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.