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ANVISA registration 82195309105Active

Guide Wire

ANVISA Registration Number: 82195309105PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDAHUNAN ENDOVASCULAR DEVICE CO., LTD.Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Hidrofílico
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Risk class
Class II
Registration details
Registration Number
82195309105
Process Number
25351076905202649
CNPJ
27939884000109
Company information
Registration Holder
PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
HUNAN ENDOVASCULAR DEVICE CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
May 18, 2026
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 82195309105 and manufactured by HUNAN ENDOVASCULAR DEVICE 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.