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ANVISA registration 81040530065Active

Guide Wire

ANVISA Registration Number: 81040530065PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO LTDA MEMTW ENDOSCOPIERisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO GUIA MTW
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Risk class
Class II
Registration details
Registration Number
81040530065
Process Number
25351597426201932
CNPJ
13179728000174
Company information
Registration Holder
PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO LTDA ME
Manufacturer
MTW ENDOSCOPIE
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Nov 18, 2019
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 81040530065 and manufactured by MTW ENDOSCOPIE. The registration is held by PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO LTDA ME 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.