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ANVISA registration 82195309004Active

Guide Wire

ANVISA Registration Number: 82195309004PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDACARDIOLINK SCIENCE (SHENZHEN) MEDICAL TECHNOLOGY DEVELOPMENT CO., LTD.Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Micro Fio-Guia
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Risk class
Class II
Registration details
Registration Number
82195309004
Process Number
25351114720202488
CNPJ
27939884000109
Company information
Registration Holder
PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
CARDIOLINK SCIENCE (SHENZHEN) MEDICAL TECHNOLOGY DEVELOPMENT CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Apr 01, 2024
Status
Active
Official value: VIGENTE
Last Updated
08/19/2026 19:00:01
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 82195309004 and manufactured by CARDIOLINK SCIENCE (SHENZHEN) MEDICAL TECHNOLOGY DEVELOPMENT CO., LTD.. The registration is held by PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES 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.