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ANVISA registration 82036520054Valid until May 11, 2036

CARDIOVASCULAR GUIDE WIRE

ANVISA Registration Number: 82036520054QLS - QUALITY LIFE SCIENCES IMPORTAÇÃO E EXPORTAÇÃO LTDASHUNMEI MEDICAL CO., LTDRisk Class IV
Verified
Device names
Technical name
CARDIOVASCULAR GUIDE WIRE
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PT: FIO GUIA CARDIOVASCULAR
Commercial name
FIO GUIA PTCA (SHUN PI)
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Risk class
Class IV
Registration details
Registration Number
82036520054
Process Number
25351378070202405
CNPJ
37182605000150
Company information
Registration Holder
QLS - QUALITY LIFE SCIENCES IMPORTAÇÃO E EXPORTAÇÃO LTDA
Manufacturer
SHUNMEI MEDICAL CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
May 11, 2026
Validity
11/05/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 82036520054 and manufactured by SHUNMEI MEDICAL CO., LTD. The registration is held by QLS - QUALITY LIFE SCIENCES IMPORTAÇÃO E EXPORTAÇÃO LTDA with validity until May 11, 2036.

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.