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ANVISA registration 10413960242Valid until Jul 17, 2033

CARDIOVASCULAR GUIDE WIRE

ANVISA Registration Number: 10413960242SCITECH PRODUTOS MEDICOS SASHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTDRisk Class IV
Verified
Device names
Technical name
CARDIOVASCULAR GUIDE WIRE
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PT: FIO GUIA CARDIOVASCULAR
Commercial name
FIO GUIA HIDROFILICO 014”
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Risk class
Class IV
Registration details
Registration Number
10413960242
Process Number
25351540777202277
CNPJ
01437707000122
Company information
Registration Holder
SCITECH PRODUTOS MEDICOS SA
Manufacturer
SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jul 17, 2023
Validity
17/07/2033
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10413960242 and manufactured by SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD. The registration is held by SCITECH PRODUTOS MEDICOS SA with validity until Jul 17, 2033.

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.