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ANVISA registration 80446140023Active

Guide Wire

ANVISA Registration Number: 80446140023SMT IMPORTADORA E DISTRIBUIDORA DE PRODUTOS HOSPITALARES LTDA.SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.Risk Class I
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Hidrofilico SM
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Risk class
Class I
Registration details
Registration Number
80446140023
Process Number
25351080417201703
CNPJ
08862233000105
Company information
Registration Holder
SMT IMPORTADORA E DISTRIBUIDORA DE PRODUTOS HOSPITALARES LTDA.
Manufacturer
SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Mar 20, 2017
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 I medical device is registered under ANVISA number 80446140023 and manufactured by SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.. The registration is held by SMT IMPORTADORA E DISTRIBUIDORA 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.