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ANVISA registration 10309090032Active

Guide Wire

ANVISA Registration Number: 10309090032CLINICAL THINKS COMÉRCIO DE PROD. E EQUIP. CIRÚRGICOS LTDAINSITU TECHNOLOGIES, INCRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Lobella
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Risk class
Class II
Registration details
Registration Number
10309090032
Process Number
25351306794201809
CNPJ
85472199000103
Company information
Registration Holder
CLINICAL THINKS COMÉRCIO DE PROD. E EQUIP. CIRÚRGICOS LTDA
Manufacturer
INSITU TECHNOLOGIES, INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Aug 20, 2018
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 II medical device is registered under ANVISA number 10309090032 and manufactured by INSITU TECHNOLOGIES, INC. The registration is held by CLINICAL THINKS COMÉRCIO DE PROD. E EQUIP. CIRÚRGICOS 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.