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ANVISA registration 80447719011Active

Guide Wire

ANVISA Registration Number: 80447719011HOMACC COMERCIO DE MATERIAL MEDICO HOSPITALAR LTDATIANCK MEDICAL CO., LTDRisk Class II
Verified
Device names
Technical name
Guide Wire
View exact technical-name matches →
PT: Fio Guia
Commercial name
Fio Guia Hidrofílico Atria
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Risk class
Class II
Registration details
Registration Number
80447719011
Process Number
25351054314202611
CNPJ
07797579000104
Company information
Registration Holder
HOMACC COMERCIO DE MATERIAL MEDICO HOSPITALAR LTDA
Manufacturer
TIANCK MEDICAL CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Apr 13, 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 80447719011 and manufactured by TIANCK MEDICAL CO., LTD. The registration is held by HOMACC COMERCIO DE MATERIAL MEDICO HOSPITALAR 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.