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ANVISA registration 82214249022Active

Guide Wire

ANVISA Registration Number: 82214249022LYNX PRODUTOS MEDICOS LTDA.YANGZHOU FARTLEY MEDICAL INSTRUMENT TECHNOLOGY CO. LTD.Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Hydrus Fio Guia Hidrofilico
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Risk class
Class II
Registration details
Registration Number
82214249022
Process Number
25351106733202645
CNPJ
08587310000166
Company information
Registration Holder
LYNX PRODUTOS MEDICOS LTDA.
Manufacturer
YANGZHOU FARTLEY MEDICAL INSTRUMENT TECHNOLOGY CO. LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 29, 2026
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 82214249022 and manufactured by YANGZHOU FARTLEY MEDICAL INSTRUMENT TECHNOLOGY CO. LTD.. The registration is held by LYNX PRODUTOS MEDICOS 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.