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ANVISA registration 10350539010Active

Guide Wire

ANVISA Registration Number: 10350539010LINE LIFE CARDIOVASCULAR COM DE PROD MED E HOSP LTDATELEFLEX MEDICAL INCORPORATEDRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio-guia R350
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Risk class
Class II
Registration details
Registration Number
10350539010
Process Number
25351431744201608
CNPJ
01197835000146
Company information
Registration Holder
LINE LIFE CARDIOVASCULAR COM DE PROD MED E HOSP LTDA
Manufacturer
TELEFLEX MEDICAL INCORPORATED
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Nov 28, 2016
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 10350539010 and manufactured by TELEFLEX MEDICAL INCORPORATED. The registration is held by LINE LIFE CARDIOVASCULAR COM DE PROD MED E HOSP 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.