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ANVISA registration 80253920011Active

Guide Wire

ANVISA Registration Number: 80253920011INTENSIVEMED IMPORTAÇÃO E COMÉRCIO LTDATIANCK MEDICAL CO., LTDRisk Class I
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio guia teflonado Tianck Medical
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Risk class
Class I
Registration details
Registration Number
80253920011
Process Number
25351061209202123
CNPJ
02937303000160
Company information
Registration Holder
INTENSIVEMED IMPORTAÇÃO E COMÉRCIO LTDA
Manufacturer
TIANCK MEDICAL CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jan 06, 2022
Status
Active
Official value: VIGENTE
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 80253920011 and manufactured by TIANCK MEDICAL CO., LTD. The registration is held by INTENSIVEMED IMPORTAÇÃO E COMÉRCIO 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.